RSS-Feed abonnieren

DOI: 10.5935/2526-8732.20210025
Colorectal cancer biomarkers and their impact on the clinical practice
Biomarcadores de câncer colorretal e seu impacto na prática clínicaAuthors
Financial support: None to declare.

ABSTRACT
Colorectal cancer (CRC) holds third place in the global ranking of malignancies worldwide. Patients with CRC commonly show distinct outcomes and treatment responses due to their biological features and tumoral biomarkers. This review explores the repertoire of molecular biomarkers in CRC, comprised of chromosomal aberrations and genomic instability and genetic mutations. We also underline the stratification of CRC patients into four clinically defined subsets: CMS1 (MSI, immune); CMS2 (canonical); CMS3 (metabolic); and CMS4 (mesenchymal), as well as novel techniques to be applied very soon in the field, such as cell-free DNA, tumor mutational burden, and microbiome profiling.
RESUMO
O câncer colorretal (CCR) ocupa o terceiro lugar no ranking mundial de doenças malignas. Pacientes com CCR geralmente apresentam resultados e respostas ao tratamento distintos devido às suas características biológicas e biomarcadores tumorais. Esta revisão explora o repertório de biomarcadores moleculares no CCR, composto por aberrações cromossômicas e instabilidade genômica e mutações genéticas. Também destacamos a estratificação dos pacientes com CCR em quatro subconjuntos clinicamente definidos: CMS1 (MSI, imune); CMS2 (canônico); CMS3 (metabólico); e CMS4 (mesenquimal), bem como novas técnicas a serem aplicadas muito em breve na área, como DNA livre de células, carga mutacional tumoral e perfil do microbioma.
Keywords:
Biomarcadores - Genômica - Prognóstico - Agentes antineoplásicos - Neoplasias colorretais.Descritores:
Biomarcadores - Genômica - Prognóstico - Agentes antineoplásicos - Neoplasias colorretais.FUNDING INFORMATION
This work was supported by Instituto COI.
Conflict of Interests
The authors declare no conflict of interest relevant to this manuscript.
AUTHOR CONTRIBUTIONS
Conceptualization: J.C, A.P.V, L.H.A and F.M.A.C.V. Writing-original draft preparation: J.C, A.P.V and F.M.A.C.V.
Writing-review and editing: J.C, A.P.V, K.B.A, L.H.A and F.M.A.C.V.
All authors have read and agreed to the final version of the manuscript.
Publikationsverlauf
Eingereicht: 10. März 2021
Angenommen: 25. Juni 2021
Artikel online veröffentlicht:
16. September 2021
© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
James Crespo, Ana Paula Victorino, Kelly Araujo, Luiz Henrique Araujo, Fernando Meton de Alencar Camara Vieira. Colorectal cancer biomarkers and their impact on the clinical practice. Brazilian Journal of Oncology 2021; 17: e-20210025.
DOI: 10.5935/2526-8732.20210025
-
REFERENCES
- 1
International Agency for Research on Cancer (IARC); World Health Organization (WHO).
Global cancer observatory (GCO) [Internet]. Geneva: IARC/WHO;; 2020. ; [access in
2020 Sep 22]. Available from: https://gco.iarc.fr
Reference Ris Wihthout Link
- 2
National Cancer Institute (NIH).
Cancer stat facts: colorectal cancer [Internet]. Bethesda: NIH;; 2020. ;[access in
2020 May 17]. Available from: https://seer.cancer.gov/statfacts/html/colorect.html
Reference Ris Wihthout Link
- 3
Kocarnik JM,
Shiovitz S,
Phipps AI.
Molecular phenotypes of colorectal cancer and potential clinical applications. Gastroenterol
Rep (Oxf) 2015; 3 (04) 269-276 https://doi.org/10.1093/gastro/gov046
Reference Ris Wihthout Link
- 4
Loree JM,
Pereira AAL,
Lam M,
Willauer AN,
Raghav K,
Dasari A.
et al.
Classifying colorectal cancer by tumor location rather than sidedness highlights a
continuum in mutation profiles and consensus molecular subtypes. Clin Cancer Res 2018;
Mar; 24 (05) 1062-1072 https://doi.org/10.1158/1078-0432.CCR-17-2484
Reference Ris Wihthout Link
- 5
Wong R.
Proximal tumors are associated with greater mortality in colon cancer. J Gen Intern
Med 2010; Jul; 25: 1157-1163 https://doi.org/10.1007/s11606-010-1460-4
Reference Ris Wihthout Link
- 6
Missiaglia E,
Jacobs B,
D'Ario G,
Di Narzo AF,
Soneson C,
Budinska E.
et al.
Distal and proximal colon cancers differ in terms of molecular, pathological, and
clinical features. Ann Oncol 2014; Oct; 25 (10) 1995-2001 https://doi.org/10.1093/annonc/mdu275
Reference Ris Wihthout Link
- 7
Wang CB,
Shahjehan F,
Merchea A,
Li Z,
BekaiiSaab TS,
Grothey A.
et al.
Impact of tumor location and variables associated with overall survival in patients
with colorectal cancer: a Mayo clinic colon and rectal cancer registry study. Front
Oncol 2019; 9: 76 https://doi.org/10.3389/fonc.2019.00076
Reference Ris Wihthout Link
- 8
Wang B,
Yang J,
Li S,
Lv M,
Chen Z,
Li E.
et al.
Tumor location as a novel high risk parameter for stage II colorectal cancers. PLoS
One 2017; 12 (06) e0179910 https://doi.org/10.1371/journal.pone.0179910
Reference Ris Wihthout Link
- 9
Warschkow R,
Sulz MC,
Marti L,
Tarantino I,
Schmied BM,
Cerny T.
et al.
Better survival in right-sided versus left-sided stage I - III colon cancer patients.
BMC Cancer 2016; Jul; 16: 554 https://doi.org/10.1186/s12885-016-2412-0
Reference Ris Wihthout Link
- 10
Yamashita S,
Brudvik KW,
Kopetz SE,
Maru D,
Clarke CN,
Passot G.
et al.
Embryonic origin of primary colon cancer predicts pathologic response and survival
in patients undergoing resection for colon cancer liver metastases. Ann Surg 2018;
Mar; 267 (03) 514-520 https://doi.org/10.1097/SLA.0000000000002087
Reference Ris Wihthout Link
- 11
Sanchez-Alcoholado L,
Ramos-Molina B,
Otero A,
Laborda-Illanes A,
Ordonez R,
Medina JA.
et al.
The role of the gut microbiome in colorectal cancer development and therapy response.
Cancers (Basel) 2020; 12 (06) 1406 https://doi.org/10.3390/cancers12061406
Reference Ris Wihthout Link
- 12
Dahmus JD,
Kotler DL,
Kastenberg DM,
Kistler CA.
The gut microbiome and colorectal cancer: a review of bacterial pathogenesis. J Gastrointest
Oncol 2018; 9 (04) 769-777 https://doi.org/10.21037/jgo.2018.04.07
Reference Ris Wihthout Link
- 13
Verhulst J,
Ferdinande L,
Demetter P,
Ceelen W.
Mucinous subtype as prognostic factor in colorectal cancer: a systematic review and
meta-analysis. J Clin Pathol 2012; 65 (05) 381-388 https://doi.org/10.1136/jclinpath-2011-200340
Reference Ris Wihthout Link
- 14
Hugen N,
Van de Velde CJH,
Wilt JHW,
Nagtegaal ID.
Metastatic pattern in colorectal cancer is strongly influenced by histological subtype.
Ann Oncol 2014; 25: 651-657 https://doi.org/10.1093/annonc/mdt591
Reference Ris Wihthout Link
- 15
Maisano R,
Azzarello D,
Maisano M,
Mafodda A,
Bottari M,
Egitto G.
et al.
Mucinous histology of colon cancer predicts poor outcomes with FOLFOX regimen in metastatic
colon cancer. J Chemother 2012; Aug; 24 (04) 212-216
Reference Ris Wihthout Link
- 16
McCawley N,
Clancy C,
O'Neill BD,
Deasy J,
McNamara DA,
Burke JP.
Mucinous rectal adenocarcinoma is associated with a poor response to neoadjuvant chemoradiotherapy:
a systematic review and meta-analysis. Dis Colon Rectum 2016; Dec; 59 (12) 1200-1208
https://doi.org/10.1097/DCR.0000000000000635
Reference Ris Wihthout Link
- 17
Thota R,
Fang X,
Subbiah S.
Clinicopathological features and survival outcomes of primary signet ring cell and
mucinous adenocarcinoma of colon: retrospective analysis of VACCR database. J Gastrointest
Oncol 2014; Feb; 5 (01) 18-24
Reference Ris Wihthout Link
- 18
Yun SO,
Cho YB,
Lee WY,
Kim HC,
Yun SH,
Park YA.
et al.
Clinical significance of signet-ring-cell colorectal cancer as a prognostic factor.
Ann Coloproctol 2017; Dec; 33 (06) 232-238 https://doi.org/10.3393/ac.2017.33.6.232
Reference Ris Wihthout Link
- 19
Gao Y,
Wang J,
Zhou Y,
Sheng S,
Qian SY,
Huo X.
Evaluation of Serum CEA, CA19- 9, CA72-4, CA125 and ferritin as diagnostic markers
and factors of clinical parameters for colorectal cancer. Sci Rep 2018; Feb; 8: 2732
https://doi.org/10.1038/s41598-018-21048-y
Reference Ris Wihthout Link
- 20
Huang CJ,
Jiang JK,
Chang SC,
Lin JK,
Yang SH.
Serum CA125 concentration as a predictor of peritoneal dissemination of colorectal
cancer in men and women. Medicine (Baltimore) 2016; 95 (47) e5177 https://doi.org/10.1097/MD.0000000000005177
Reference Ris Wihthout Link
- 21
Brouwer NPM,
Bos A,
Lemmens V,
Tanis PJ,
Hugen N,
Nagtegaal ID.
et al.
An overview of 25 years of incidence, treatment and outcome of colorectal cancer patients.
Int J Cancer 2018; Aug; 143 (11) 2758-2766 https://doi.org/10.1002/ijc.31785
Reference Ris Wihthout Link
- 22
Messersmith WA.
NCCN guidelines updates: management of metastatic colorectal cancer. J Natl Compr
Canc Netw 2019; May; 17 (05) 599-601
Reference Ris Wihthout Link
- 23
Brown KGM,
Solomon MJ,
Mahon K,
O'Shan nassy S.
Management of colorectal cancer. BMJ 2019; 366: l4561 https://doi.org/10.1136/bmj.l4561
Reference Ris Wihthout Link
- 24
Vogel A,
Hofheinz RD,
Kubicka S,
Arnold D.
Treatment decisions in metastatic colorectal cancer - Beyond first and second line
combination therapies. Cancer Treat Rev 2017; Sep; 59: 54-60 https://doi.org/10.1016/j.ctrv.2017.04.007
Reference Ris Wihthout Link
- 25
Xie YH,
Chen YX,
Fang JY.
Comprehensive review of targeted therapy for colorectal cancer. Signal Transduct Target
Ther 2020; 5: 22 https://doi.org/10.1038/s41392-020-0116-z
Reference Ris Wihthout Link
- 26
Fearon ER,
Vogelstein B. A.
genetic model for colorectal tumorigenesis. Cell 1990; Jun; 61 (05) 759-767 https://doi.org/10.1016/0092-8674(90)90186-i
Reference Ris Wihthout Link
- 27
Grady WM,
Carethers JM.
Genomic and epigenetic instability in colorectal cancer pathogenesis. Gastroenterology
2008; Oct; 135 (04) 1079-1099
Reference Ris Wihthout Link
- 28
Walther A,
Houlston R,
Tomlinson I.
Association between chromosomal instability and prognosis in colorectal cancer: a
meta-analysis. Gut 2008; 57 (07) 941-950 https://doi.org/10.1136/gut.2007.135004
Reference Ris Wihthout Link
- 29
Hoevenaar WHM,
Janssen A,
Quirindongo AI,
Ma H,
Klaasen SJ,
Teixeira A.
et al.
Degree and site of chromosomal instability define its oncogenic potential. Nat Commun
2020; 11: 1501 https://doi.org/10.1038/s41467-020-15279-9
Reference Ris Wihthout Link
- 30
Evrard C,
Tachon G,
Randrian V,
Karayan-Tapon L,
Tougeron D.
Microsatellite instability: diagnosis, heterogeneity, discordance, and clinical impact
in colorectal cancer. Cancers (Basel) 2019; 11 (10) 1567 https://doi.org/10.3390/cancers11101567
Reference Ris Wihthout Link
- 31
Kim GP,
Colangelo LH,
Wieand HS,
Paik S,
Kirsch IR,
Wolmark N.
et al.
Prognostic and predictive roles of high-degree microsatellite instability in colon
cancer: a National Cancer Institute-National Surgical Adjuvant Breast and Bowel Project
Collaborative Study. J Clin Oncol 2007; 25 (07) 767-772 https://doi.org/10.1200/JCO.2006.05.8172
Reference Ris Wihthout Link
- 32
Halvarsson B,
Anderson H,
Domanska K,
Lindmark G,
Nilbert M.
Clinicopathologic factors identify sporadic mismatch repair-defective colon cancers.
Am J Clin Pathol 2008; 129 (02) 238-244 https://doi.org/10.1309/0PP5GDRTXUDVKAWJ
Reference Ris Wihthout Link
- 33
Cunningham JM,
Christensen ER,
Tester DJ,
Kim CY,
Roche PC,
Burgart LJ.
et al.
Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability.
Cancer Res 1998; Aug; 58 (15) 3455-3460
Reference Ris Wihthout Link
- 34
Giardiello FM,
Allen JI,
Axilbund JE,
Boland CR,
Burke CA,
Burt RW.
et al.
Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement
by the US Multi-Society Task Force on colorectal cancer. Gastroenterology 2014; Aug;
147 (02) 502-526
Reference Ris Wihthout Link
- 35
Ribic CM,
Sargent DJ,
Moore MJ,
Thibodeau SN,
French AJ,
Goldberg RM.
et al.
Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based
adjuvant chemotherapy for colon cancer. N Engl J Med 2003; Jul; 349: 247-257 https://doi.org/10.1056/NEJMoa022289
Reference Ris Wihthout Link
- 36
Sargent DJ,
Marsoni S,
Monges G,
Thibodeau SN,
Labianca R,
Hamilton SR.
et al.
Defective mismatch repair as a predictive marker for lack of efficacy of fluorouracil-based
adjuvant therapy in colon cancer. J Clin Oncol 2010; 28 (20) 3219-3226 https://doi.org/10.1200/JCO.2009.27.1825
Reference Ris Wihthout Link
- 37
Cohen R,
Taieb J,
Fiskum J,
Yothers G,
Goldberg R,
Yoshino T.
et al.
Microsatellite instability in patients with stage III colon cancer receiving fluoropyrimidine
with or without oxaliplatin: an ACCENT pooled analysis of 12 adjuvant trials. J Clin
Oncol 2021; 39 (06) 642-651 https://doi.org/10.1200/JCO.20.01600
Reference Ris Wihthout Link
- 38
Roth AD,
Tejpar S,
Delorenzi M,
Yan P,
Fiocca R,
Klingbiel D.
et al.
Prognostic role of KRAS and BRAF in stage II and III resected colon cancer: results
of the translational study on the PETACC-3, EORTC 40993, SAKK 60-00 trial. J Clin
Oncol 2010; 28 (03) 466-474 https://doi.org/10.1200/JCO.2009.23.3452
Reference Ris Wihthout Link
- 39
Koopman M,
Kortman GA,
Mekenkamp L,
Ligtenberg MJ,
Hoogerbrugge N,
Antonini NF.
et al.
Deficient mismatch repair system in patients with sporadic advanced colorectal cancer.
Br J Cancer 2009; 100: 266-273 https://doi.org/10.1038/sj.bjc.6604867
Reference Ris Wihthout Link
- 40
Sinicrope FA,
Mahoney MR,
Smyrk TC,
Thibodeau SN,
Warren RS,
Bertagnolli MM.
et al.
Prognostic impact of deficient DNA mismatch repair in patients with stage III colon
cancer from a randomized trial of FOLFOX-based adjuvant chemotherapy. J Clin Oncol
2013; 31 (29) 3664-3672 https://doi.org/10.1200/JCO.2013.48.9591
Reference Ris Wihthout Link
- 41
Webber EM,
Kauffman TL,
O'Connor E,
Goddard KA.
Systematic review of the predictive effect of MSI status in colorectal cancer patients
undergoing 5FUbased chemotherapy. BMC Cancer 2015; 15: 156 https://doi.org/10.1186/s12885-015-1093-4
Reference Ris Wihthout Link
- 42
Shia J.
Immunohistochemistry versus microsatellite instability testing for screening colorectal
cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part
I. The utility of immunohistochemistry. J Mol Diagn 2008; 10 (04) 293-300
Reference Ris Wihthout Link
- 43
B, Lagorce-Pages C.
et al.
Type, density, and location of immune cells within human colorectal tumors predict
clinical outcome. Science 2006; 313 (5795) 1960-1964 https://doi.org/10.1126/science.1129139
Reference Ris Wihthout Link
- 44
Li Y,
Liang L,
Dai W,
Cai G,
Xu Y,
Li X.
et al.
Prognostic impact of programed cell death-1 (PD-1) and PD-ligand 1 (PD-L1) expression
in cancer cells and tumor infiltrating lymphocytes in colorectal cancer. Mol Cancer
2016; Aug; 15: 55 https://doi.org/10.1186/s12943-016-0539-x
Reference Ris Wihthout Link
- 45
Llosa NJ,
Cruise M,
Tam A,
Wicks EC,
Hechenblei kner EM,
Taube JM.
et al.
The vigorous immune microenvironment of microsatellite instable colon cancer is balanced
by multiple counter-inhibitory checkpoints. Cancer Discov 2015; 5: 43-51 https://doi.org/10.1158/2159-8290.CD-14-0863
Reference Ris Wihthout Link
- 46
Le DT,
Uram JN,
Wang H,
Bartlett BR,
Kemberling H,
Eyring AD.
et al.
PD-1 blockade in tumors with mismatch-repair deficiency. N Engl J Med 2015; Jun;
372: 2509-2520 https://doi.org/10.1056/NEJMoa1500596
Reference Ris Wihthout Link
- 47
Overman MJ,
McDermott R,
Leach JL,
Lonardi S,
Lenz HJ,
Morse MA.
et al.
Nivolumab in patients with metastatic DNA mismatch repair-deficient or microsatellite
instability-high colorectal cancer (CheckMate 142): an open-label, multicentre, phase
2 study. Lancet Oncol 2017; Sep; 18 (09) 1182-1191 https://doi.org/10.1016/S1470-2045(17)30422-9
Reference Ris Wihthout Link
- 48
André T,
Shiu KK,
Kim TW,
Jensen BV,
Jensen LH,
Punt C.
et al.
Pembrolizumab in microsatellite-instability-high advanced colorectal cancer. N Engl
J Med 2020; 383: 2207-2218 https://doi.org/10.1056/NEJMoa2017699
Reference Ris Wihthout Link
- 49
Vogelstein B,
Fearon ER,
Hamilton SR,
Kern SE,
Preisinger AC,
Leppert M.
et al.
Genetic alterations during colorectal-tumor development. N Engl J Med 1988; Sep;
319: 525-532 https://doi.org/10.1056/NEJM198809013190901
Reference Ris Wihthout Link
- 50
Walther A,
Johnstone E,
Swanton C,
Midgley R,
Tomlinson I,
Kerr D.
Genetic prognostic and predictive markers in colorectal cancer. Nat Rev Cancer 2009;
9: 489-499 https://doi.org/10.1038/nrc2645
Reference Ris Wihthout Link
- 51
Drilon A,
Laetsch TW,
Kummar S,
DuBois SG,
Lassen UN,
Demetri GD.
et al.
Efficacy of larotrectinib in TRK fusion-positive cancers in adults and children. N
Engl J Med 2018; 378: 731-739 https://doi.org/10.1056/NEJMoa1714448
Reference Ris Wihthout Link
- 52
Doebele RC,
Drilon A,
Paz-Ares L,
Siena S,
Shaw AT,
Farago AF.
et al.
Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours:
integrated analysis of three phase 1-2 trials. Lancet Oncol 2020; Feb; 21 (02) 271-282
https://doi.org/10.1016/S1470-2045(19)30691-6
Reference Ris Wihthout Link
- 53
Pietrantonio F,
Di Nicolantonio F,
Schrock AB,
Lee J,
Tejpar S,
Sartore-Bianchi A.
et al.
ALK, ROS1, and NTRK rearrangements in metastatic colorectal cancer. J Natl Cancer
Inst 2017; 109: djx089 https://doi.org/10.1093/jnci/djx089
Reference Ris Wihthout Link
- 54
Pagani F,
Randon G,
Guarini V,
Raimondi A,
Prisciandaro M,
Lobefaro R.
et al.
The landscape of actionable gene fusions in colorectal cancer. Int J Mol Sci 2019;
20
Reference Ris Wihthout Link
- 55
Siena S,
Sartore-Bianchi A,
Di Nicolantonio F,
Balfour J,
Bardelli A.
Biomarkers predicting clinical outcome of epidermal growth factor receptor-targeted
therapy in metastatic colorectal cancer. J Natl Cancer Inst 2009; Oct; 101 (19) 1308-1324
https://doi.org/10.1093/jnci/djp280
Reference Ris Wihthout Link
- 56
Danielsen SA,
Lind GE,
Bjornslett M,
Meling GI,
Rognum TO,
Heim S.
et al.
Novel mutations of the suppressor gene PTEN in colorectal carcinomas stratified by
microsatellite instability- and TP53 mutation-status. Hum Mutat 2008; 29 (11) E25262
https://doi.org/10.1002/humu.20860
Reference Ris Wihthout Link
- 57
Razis E,
Briasoulis E,
Vrettou E,
Skarlos DV,
Papamichael D,
Kostopoulos I.
et al.
Potential value of PTEN in predicting cetuximab response in colorectal cancer: an
exploratory study. BMC Cancer 2008; Aug; 8: 234 https://doi.org/10.1186/1471-2407-8-234
Reference Ris Wihthout Link
- 58
Sartore-Bianchi A,
Martini M,
Molinari F,
Veronese S,
Nichelatti M,
Artale S.
et al.
PIK3CA mutations in colorectal cancer are associated with clinical resistance to EGFR-targeted
monoclonal antibodies. Cancer Res 2009; 69 (05) 1851-1857 https://doi.org/10.1158/0008-5472.CAN-08-2466
Reference Ris Wihthout Link
- 59
Ogino S,
Liao X,
Imamura Y,
Yamauchi M,
McCleary NJ,
Ng K.
et al.
Predictive and prognostic analysis of PIK3CA mutation in stage III colon cancer intergroup
trial. J Natl Cancer Inst 2013; 105 (23) 178998 https://doi.org/10.1093/jnci/djt298
Reference Ris Wihthout Link
- 60
Price TJ,
Hardingham JE,
Lee CK,
Townsend AR,
Wrin JW,
Wilson K.
et al.
Prognostic impact and the relevance of PTEN copy number alterations in patients with
advanced colorectal cancer (CRC) receiving bevacizumab. Cancer Med 2013; Mar; 2 (03)
277-285 https://doi.org/10.1002/cam4.75
Reference Ris Wihthout Link
- 61
Adjei AA.
Blocking oncogenic Ras signaling for cancer therapy. J Natl Cancer Inst 2001; 93:
1062-1074 https://doi.org/10.1093/jnci/93.14.1062
Reference Ris Wihthout Link
- 62
Grothey A,
Sargent D.
Overall survival of patients with advanced colorectal cancer correlates with availability
of fluorouracil, irinotecan, and oxaliplatin regardless of whether doublet or single-agent
therapy is used first line. J Clin Oncol 2005; 23 (36) 94412 https://doi.org/10.1200/JCO.2005.04.4792
Reference Ris Wihthout Link
- 63
Karapetis CS,
Khambata-Ford S,
Jonker DJ,
O'Callaghan CJ,
Tu D,
Tebbutt NC.
et al.
K-ras mutations and benefit from cetuximab in advanced colorectal cancer. N Engl J
Med 2008; Oct; 359: 1757-1765 https://doi.org/10.1056/NEJMoa0804385
Reference Ris Wihthout Link
- 64
Douillard JY,
Oliner KS,
Siena S,
Tabernero J,
Burkes R,
Barugel M.
et al.
Panitumumab-FOLFOX4 treatment and RAS mutations in colorectal cancer. N Engl J Med
2013; Sep; 369: 1023-1034 https://doi.org/10.1056/NEJMoa1305275
Reference Ris Wihthout Link
- 65
Ferreira CG,
Aran V,
Zalcberg-Renault I,
Victorino AP,
Salem JH,
Bonamino MH.
et al.
KRAS mutations: variable incidences in a Brazilian cohort of 8,234 metastatic colorectal
cancer patients. BMC Gastroenterol 2014; Apr; 14: 73 https://doi.org/10.1186/1471-230X-14-73
Reference Ris Wihthout Link
- 66
Pereira AAL,
Fernandes GDS,
Braga GTP,
Marchetti KR,
Mascarenhas CDC,
Gumz B.
et al.
Differences in pathology and mutation status among colorectal cancer patients younger
than, older than, and of screening age. Clin Colorectal Cancer 2020; 19 (04) e264-e71
https://doi.org/10.1016/j.clcc.2020.06.004
Reference Ris Wihthout Link
- 67
Heinemann V,
Von Weikersthal LF,
Decker T,
Ki ani A,
Vehling-Kaiser U,
Al-Batran SE.
et al.
FOLFIRI plus cetuximab versus FOLFIRI plus bevacizumab as first-line treatment for
patients with metastatic colorectal cancer (FIRE-3): a randomised, open-label, phase
3 trial. Lancet Oncol 2014; 15 (10) 1065-1075 https://doi.org/10.1016/S1470-2045(14)70330-4
Reference Ris Wihthout Link
- 68
Hong DS,
Fakih MG,
Strickler JH,
Desai J,
Durm GA,
Shapiro GI.
et al.
KRASG12C inhibition with sotorasib in advanced solid tumors. N Engl J Med 2020; Sep;
383: 1207-1217 https://doi.org/10.1056/NEJMoa1917239
Reference Ris Wihthout Link
- 69
Johnson ML,
Ou SHI,
Barve M,
Rybkin II,
Papadopoulos KP,
Leal TA.
et al.
KRYSTAL-1: activity and safety of adagrasib (MRTX849) in patients with colorectal
cancer (CRC) and other solid tumors harboring a KRAS G12C mutation. Eur J Cancer 2020;
138 (Suppl 2): S2 https://doi.org/10.1016/S0959-8049(20)31077-7
Reference Ris Wihthout Link
- 70
Pereira AA,
Rego JF,
Morris V,
Overman MJ,
Eng C,
Garrett CR.
et al.
Association between KRAS mutation and lung metastasis in advanced colorectal cancer.
Br J Cancer 2015; 112: 424-428 https://doi.org/10.1038/bjc.2014.619
Reference Ris Wihthout Link
- 71
Tol J,
Nagtegaal ID,
Punt CJ.
BRAF mutation in metastatic colorectal cancer. N Engl J Med 2009; 361: 98-99 https://doi.org/10.1056/NEJMc0904160
Reference Ris Wihthout Link
- 72
Jones JC,
Renfro LA,
Al-Shamsi HO,
Schrock AB,
Rankin A,
Zhang BY.
et al.
(Non-V600) BRAF mutations define a clinically distinct molecular subtype of metastatic
colorectal cancer. J Clin Oncol 2017; 35 (23) 2624-2630 https://doi.org/10.1200/JCO.2016.71.4394
Reference Ris Wihthout Link
- 73
Farina-Sarasqueta A,
Van Lijnschoten G,
Moerland E,
Creemers GJ,
Lemmens V,
Rutten HJT.
et al.
The BRAF V600E mutation is an independent prognostic factor for survival in stage
II and stage III colon cancer patients. Ann Oncol 2010; Dec; 21 (12) 2396-2402
Reference Ris Wihthout Link
- 74
Gray RG,
Quirke P,
Handley K,
Lopatin M,
Magill L,
Baehner FL.
et al.
Validation study of a quantitative multigene reverse transcriptase-polymerase chain
reaction assay for assessment of recurrence risk in patients with stage II colon cancer.
J Clin Oncol 2011; 29 (35) 4611-4619 https://doi.org/10.1200/JCO.2010.32.8732
Reference Ris Wihthout Link
- 75
Van Cutsem E,
Kohne CH,
Lang I,
Folprecht G,
Nowacki MP,
Cascinu S.
et al.
Cetuximab plus irinotecan, fluorouracil, and leucovorin as firstline treatment for
metastatic colorectal cancer: updated analysis of overall survival according to tumor
KRAS and BRAF mutation status. J Clin Oncol 2011; 29 (15) 2011-2019 https://doi.org/10.1200/JCO.2010.33.5091
Reference Ris Wihthout Link
- 76
Price TJ,
Hardingham JE,
Lee CK,
Weickhardt A,
Townsend AR,
Wrin JW.
et al.
Impact of KRAS and BRAF gene mutation status on outcomes from the phase III AGITG
MAX trial of capecitabine alone or in combination with bevacizumab and mitomycin in
advanced colorectal cancer. J Clin Oncol 2011; 29 (19) 2675-2682 https://doi.org/10.1200/JCO.2010.34.5520
Reference Ris Wihthout Link
- 77
De Roock W,
Claes B,
Bernasconi D,
De Schutter J,
Biesmans B,
Fountzilas G.
et al.
Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus
chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective
consortium analysis. Lancet Oncol 2010; 11 (08) 753-762 https://doi.org/10.1016/S1470-2045(10)70130-3
Reference Ris Wihthout Link
- 78
Kopetz S,
Grothey A,
Yaeger R,
Van Cutsem E,
Desai J,
Yoshino T.
et al.
Encorafenib, binimetinib, and cetuximab in BRAF V600E-mutated colorectal cancer. N
Engl J Med 2019; Oct; 381: 1632-1643 https://doi.org/10.1056/NEJMoa1908075
Reference Ris Wihthout Link
- 79
Hurwitz H,
Fehrenbacher L,
Novotny W,
Cartwright T,
Hainsworth J,
Heim W.
et al.
Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal
cancer. N Engl J Med 2004; Jun; 350: 2335-2342 https://doi.org/10.1056/NEJMoa032691
Reference Ris Wihthout Link
- 80
Hurwitz HI,
Tebbutt NC,
Kabbinavar F,
Giantonio BJ,
Guan ZZ,
Mitchell L.
et al.
Efficacy and safety of bevacizumab in metastatic colorectal cancer: pooled analysis
from seven randomized controlled trials. Oncologist 2013; Jul; 18 (09) 100412 https://doi.org/10.1634/theoncologist.2013-0107
Reference Ris Wihthout Link
- 81
Giantonio BJ,
Catalano PJ,
Meropol NJ,
O'Dwyer PJ,
Mitchell EP,
Alberts SR.
et al.
Bevacizumab in combination with oxaliplatin, fluorouracil, and leucovorin (FOLFOX4)
for previously treated metastatic colorectal cancer: results from the eastern cooperative
oncology group study E3200. J Clin Oncol 2007; 25 (12) 1539-1544 https://doi.org/10.1200/jco.2006.09.6305
Reference Ris Wihthout Link
- 82
Tabernero J,
Yoshino T,
Cohn AL,
Obermannova R,
Bodoky G,
Garcia-Carbonero R.
et al.
Ramucirumab versus placebo in combination with second-line FOLFIRI in patients with
metastatic colorectal carcinoma that progressed during or after first-line therapy
with bevacizumab, oxaliplatin, and a fluoropyrimidine (RAISE): a randomised, double-blind,
multicentre, phase 3 study. Lancet Oncol 2015; May; 16 (05) 499-508 https://doi.org/10.1016/S1470-2045(15)70127-0
Reference Ris Wihthout Link
- 83
Cutsem EV,
Tabernero J,
Lakomy R,
Prenen H,
Prausová J,
Macarulla T.
et al.
Addition of aflibercept to fluorouracil, leucovorin, and irinotecan improves survival
in a phase iii randomized trial in patients with metastatic colorectal cancer previously
treated with an oxaliplatin-based regimen. J Clin Oncol 2012; 30 (28) 3499-3506 https://doi.org/10.1200/jco.2012.42.8201
Reference Ris Wihthout Link
- 84
Isaksson-Mettavainio M,
Palmqvist R,
Dahlin AM,
Van Guelpen B,
Rutegard J,
Oberg A.
et al.
High SMAD4 levels appear in microsatellite instability and hypermethylated colon cancers,
and indicate a better prognosis. Int J Cancer 2012; Sep; 131 (04) 779-788 https://doi.org/10.1002/ijc.26473
Reference Ris Wihthout Link
- 85
Kim JH,
Kang GH.
Molecular and prognos tic heterogeneity of microsatellite-unstable colorectal cancer.
World J Gastroenterol 2014; Apr; 20 (15) 4230-4243 https://doi.org/10.3748/wjg.v20.i15.4230
Reference Ris Wihthout Link
- 86
Li QH,
Wang YZ,
Tu J,
Liu CW,
Yuan YJ,
Lin R.
et al.
Anti-EGFR therapy in metastatic colorectal cancer: mechanisms and potential regimens
of drug resistance. Gastroenterol Rep (Oxf) 2020; 8 (03) 179-191 https://doi.org/10.1093/gastro/goaa026
Reference Ris Wihthout Link
- 87
Sartore-Bianchi A,
Trusolino L,
Martino C,
Bencardino K,
Lonardi S,
Bergamo F.
et al.
Dual-targeted therapy with trastuzumab and lapatinib in treatment-refractory, KRAS
codon 12/13 wild-type, HER2-positive metastatic colorectal cancer (HERACLES): a proof-of-concept,
multicentre, open-label, phase 2 trial. Lancet Oncol 2016; 17 (06) 738-746 https://doi.org/10.1016/S1470-2045(16)00150-9
Reference Ris Wihthout Link
- 88
Bardelli A,
Corso S,
Bertotti A,
Hobor S,
Valtorta E,
Siravegna G.
et al.
Amplification of the MET receptor drives resistance to anti-EGFR therapies in colorectal
cancer. Cancer Discov 2013; 3 (06) 65873 https://doi.org/10.1158/2159-8290.CD-12-0558
Reference Ris Wihthout Link
- 89
Hainsworth JD,
Meric-Bernstam F,
Swanton C,
Hurwitz H,
Spigel DR,
Sweeney C.
et al.
Therapy for advanced solid tumors on the basis of molecular profiles: results from
MyPathway, an open-label, phase IIa multiple basket study. J Clin Oncol 2018; 36 (06)
536-542 https://doi.org/10.1200/JCO.2017.75.3780
Reference Ris Wihthout Link
- 90
Raghav K,
Loree JM,
Morris JS,
Overman MJ,
Yu R,
Meric-Bernstam F.
et al.
Validation of HER2 amplification as a predictive biomarker for anti-epidermal growth
factor receptor antibody therapy in metastatic colorectal cancer. JCO Precision Oncol
2019; 226: 1-13 https://doi.org/10.1200/PO.18.00226
Reference Ris Wihthout Link
- 91
Meric-Bernstam F,
Hurwitz H,
Raghav KPS,
McWilliams RR,
Fakih M,
VanderWalde A.
et al.
Pertuzumab plus trastuzumab for HER2-amplified metastatic colorectal cancer (MyPathway):
an updated report from a multicentre, open-label, phase 2a, multiple basket study.
Lancet Oncol 2019; 20 (04) 518-530 https://doi.org/10.1016/S1470-2045(18)30904-5
Reference Ris Wihthout Link
- 92
Siena S,
Bartolomeo MD,
Raghav KPS,
Masuishi T,
Loupakis F,
Kawakami H.
et al.
A phase II, multicenter, open-label study of trastuzumab deruxtecan (T-DXd; DS-8201)
in patients (pts) with HER2-expressing metastatic colorectal cancer (mCRC): DESTINY-CRC01.
J Clin Oncol 2020; 38 (15) Suppl 1 4000 https://doi.org/10.1200/JCO.2020.38.15_suppl.4000
Reference Ris Wihthout Link
- 93
Xu Y,
Huang Z,
Li C,
Zhu C,
Zhang Y,
Guo T.
et al.
Comparison of molecular, clinicopathological, and pedigree differences between lynch-like
and lynch syndromes. Front Genet 2020; 11: 991 https://doi.org/10.3389/fgene.2020.00991
Reference Ris Wihthout Link
- 94
Domingo E,
Freeman-Mills L,
Rayner E,
Glaire M,
Briggs S,
Vermeulen L.
et al.
Somatic POLE proofreading domain mutation, immune response, and prognosis in colorectal
cancer: a retrospective, pooled biomarker study. Lancet Gastroenterol Hepatol 2016;
1 (03) 207-216 https://doi.org/10.1016/S2468-1253(16)30014-0
Reference Ris Wihthout Link
- 95
Mo S,
Ma X,
Li Y,
Zhang L,
Hou T,
Han-Zhang H.
et al.
Somatic POLE exonuclease domain mutations elicit enhanced intratumoral immune responses
in stage II colorectal cancer. J Immunother Cancer 2020; 8 (02) e000881 https://doi.org/10.1136/jitc-2020-000881
Reference Ris Wihthout Link
- 96
Velcheti V,
Schalper K.
Basic overview of current immunotherapy approaches in cancer. ASCO Educ 2016; 36:
298-308 https://doi.org/10.1200/edbk_156572
Reference Ris Wihthout Link
- 97
Feng D,
Chen Z,
He X,
Huang S,
Zhang Z.
Loss of tumor intrinsic PD-L1 confers resistance to drug-induced apoptosis in human
colon cancer. Neoplasma 2020; 68 (01) 144-153 https://doi.org/10.4149/neo_2020_200531N589
Reference Ris Wihthout Link
- 98
Wang S,
Yuan B,
Wang Y,
Li M,
Liu X,
Cao J.
et al.
Clinicopathological and prognostic significance of PD-L1 expression in colorectal
cancer: a meta-analysis. Int J Colorectal Dis 2020; Sep; 36: 117-130 https://doi.org/10.1007/s00384-020-03734-4
Reference Ris Wihthout Link
- 99
Flavahan WA,
Gaskell E,
Bernstein BE.
Epigenetic plasticity and the hallmarks of cancer. Science 2017; 357 (6348) eaal2380
https://doi.org/10.1126/science.aal2380
Reference Ris Wihthout Link
- 100
Guinney J,
Dienstmann R,
Wang X,
Reynies A,
Schlicker A,
Soneson C.
et al.
The consensus molecular subtypes of colorectal cancer. Nat Med 2015; Oct; 21: 1350-1356
https://doi.org/10.1038/nm.3967
Reference Ris Wihthout Link
- 101
Dolcetti R,
Viel A,
Doglioni C,
Russo A,
Guidoboni M,
Capozzi E.
et al.
High prevalence of activated intraepithelial cytotoxic T lymphocytes and increased
neoplastic cell apoptosis in colorectal carcinomas with microsatellite instability.
Am J Pathol 1999; Jun; 154 (06) 1805-1813
Reference Ris Wihthout Link
- 102
Fessler E,
Medema JP.
Colorectal cancer subtypes: developmental origin and microenvironmental regulation.
Trends Cancer 2016; Sep; 2 (09) 505-508 https://doi.org/10.1016/j.trecan.2016.07.008
Reference Ris Wihthout Link
- 103
Ogino S,
Nosho K,
Kirkner GJ,
Kawasaki T,
Meyerhardt JA,
Loda M.
et al.
CpG island methylator phenotype, microsatellite instability, BRAF mutation and clinical
outcome in colon cancer. Gut 2009; 58 (01) 90-96 https://doi.org/10.1136/gut.2008.155473
Reference Ris Wihthout Link
- 104
Stintzing S,
Wirapati P,
Lenz HJ,
Neureiter D,
Von Weikersthal LF,
Decker T.
et al.
Consensus molecular subgroups (CMS) of colorectal cancer (CRC) and first-line efficacy
of FOLFIRI plus cetuximab or bevacizumab in the FIRE3 (AIO KRK-0306) trial. Ann Oncol
2019; Nov; 30 (11) 1796-1803
Reference Ris Wihthout Link
- 105
Sousa EMF,
Wang X,
Jansen M,
Fessler E,
Trinh A,
Rooij LP.
et al.
Poor-prognosis colon cancer is defined by a molecularly distinct subtype and develops
from serrated precursor lesions. Nat Med 2013; Apr; 19: 614-618 https://doi.org/10.1038/nm.3174
Reference Ris Wihthout Link
- 106
Alborelli I,
Generali D,
Jermann P,
Cappelletti MR,
Ferrero G,
Scaggiante B.
et al.
Cell-free DNA analysis in healthy individuals by next-generation sequencing: a proof
of concept and technical validation study. Cell Death Dis 2019; Jul; 10: 534 https://doi.org/10.1038/s41419-019-1770-3
Reference Ris Wihthout Link
- 107
Chaudhuri AA,
Chabon JJ,
Lovejoy AF,
Newman AM,
Stehr H,
Azad TD.
et al.
Early detection of molecular residual disease in localized lung cancer by circulating
tumor DNA profiling. Cancer Discov 2017; 7 (12) 1394-1403 https://doi.org/10.1158/2159-8290.CD-17-0716
Reference Ris Wihthout Link
- 108
Tie J,
Wang Y,
Tomasetti C,
Li L,
Springer S,
Kinde I.
et al.
Circulating tumor DNA analysis detects minimal residual disease and predicts recurrence
in patients with stage II colon cancer. Sci Transl Med 2016; 8 (346) 346-392 https://doi.org/10.1126/scitranslmed.aaf6219
Reference Ris Wihthout Link
- 109
Phallen J,
Sausen M,
Adleff V,
Leal A,
Hruban C,
White J.
et al.
Direct detection of early-stage cancers using circulating tumor DNA. Sci Transl Med
2017; 9 (403) eaan2415 https://doi.org/10.1126/scitranslmed.aan2415
Reference Ris Wihthout Link
- 110
Frattini M,
Gallino G,
Signoroni S,
Balestra D,
Lusa L,
Battaglia L.
et al.
Quantitative and qualitative characterization of plasma DNA identifies primary and
recurrent colorectal cancer. Cancer Lett 2008; 263 (02) 170-181 https://doi.org/10.1016/j.canlet.2008.03.021
Reference Ris Wihthout Link
- 111
Thierry AR,
Mouliere F,
El Messaoudi S,
Mollevi C,
Lopez-Crapez E,
Rolet F.
et al.
Clinical validation of the detection of KRAS and BRAF mutations from circulating tumor
DNA. Nat Med 2014; Mar; 20: 4305 https://doi.org/10.1038/nm.3511
Reference Ris Wihthout Link
- 112
Yang YC,
Wang D,
Jin L,
Yao HW,
Zhang JH,
Wang J.
et al.
Circulating tumor DNA detectable in early- and late-stage colorectal cancer patients.
Biosci Rep 2018; 38 (04) BSR20180322 https://doi.org/10.1042/BSR20180322
Reference Ris Wihthout Link
- 113
Bettegowda C,
Sausen M,
Leary RJ,
Kinde I,
Wang Y,
Agrawal N.
et al.
Detection of circulating tumor DNA in early- and late-stage human malignancies. Sci
Transl Med 2014; 6 (224) 224 https://doi.org/10.1126/scitranslmed.3007094
Reference Ris Wihthout Link
- 114
Clifton K,
Rich TA,
Parseghian C,
Raymond VM,
Dasari A,
Pereira AAL.
et al.
Identification of actionable fusions as an anti-EGFR resistance mechanism using a
circulating tumor DNA assay. JCO Precision Oncol 2019; 3
Reference Ris Wihthout Link
- 115
Reinert T,
Henriksen TV,
Christensen E,
Sharma S,
Salari R,
Sethi H.
et al.
Analysis of plasma cellfree DNA by ultradeep sequencing in patients with stages I
to III colorectal cancer. JAMA Oncol 2019; 5 (08) 1124-1131 https://doi.org/10.1001/jamaoncol.2019.0528
Reference Ris Wihthout Link
- 116
Parseghian CM,
Loree JM,
Morris VK,
Liu X,
Clifton KK,
Napolitano S.
et al.
Anti-EGFR-resistant clones decay exponentially after progression: implications for
anti-EGFR re-challenge. Ann Oncol 2019; Feb; 30 (02) 243-249
Reference Ris Wihthout Link
- 117
Dasari A,
Morris VK,
Allegra CJ,
Atreya C,
Benson AB,
Boland P.
et al.
ctDNA applications and integration in colorectal cancer: an NCI Colon and Rectal-Anal
Task Forces whitepaper. Nat Rev Clin Oncol 2020; 17: 757-770 https://doi.org/10.1038/s41571-020-0392-0
Reference Ris Wihthout Link
- 118
Dromain C,
Beigelman C,
Pozzessere C,
Duran R,
Digklia A.
Imaging of tumour response to immunotherapy. Eur Radiol Exp 2020; Jan; 4: 2 https://doi.org/10.1186/s41747-019-0134-1
Reference Ris Wihthout Link
- 119
Fabrizio DA,
George Junior TJ,
Dunne RF,
Frampton G,
Sun J,
Gowen K.
et al.
Beyond microsatellite testing: assessment of tumor mutational burden identifies subsets
of colorectal cancer who may respond to immune checkpoint inhibition. J Gastrointest
Oncol 2018; Aug; 9 (04) 610-617 https://doi.org/10.21037/jgo.2018.05.06
Reference Ris Wihthout Link
- 120
Goodman AM,
Sokol ES,
Frampton GM,
Lippman SM,
Kurzrock R.
Microsatellite-stable tumors with high mutational burden benefit from immunotherapy.
Cancer Immunol Res 2019; 7 (10) 1570-1573 https://doi.org/10.1158/2326-6066.CIR-19-0149
Reference Ris Wihthout Link
- 121
Li R,
Han D,
Shi J,
Han Y,
Tan P,
Zhang R.
et al.
Choosing tumor mutational burden wisely for immunotherapy: a hard road to explore.
Biochim Biophys Acta Rev Cancer 2020; 1874 (02) 188420 https://doi.org/10.1016/j.bbcan.2020.188420
Reference Ris Wihthout Link
- 122
Eso Y,
Seno H.
Current status of treatment with immune checkpoint inhibitors for gastrointestinal,
hepatobiliary, and pancreatic cancers. Therap Adv Gastroenterol 2020; 13: 1756284820948773
https://doi.org/10.1177/1756284820948773
Reference Ris Wihthout Link
- 123
Marabelle A,
Fakih M,
Lopez J,
Shah M,
Shapira-Frommer R,
Nakagawa K.
et al.
Association of tumour mutational burden with outcomes in patients with advanced solid
tumours treated with pembrolizumab: prospective biomarker analysis of the multicohort,
open-label, phase 2 KEYNOTE-158 study. Lancet Oncol 2020; 21 (10) 1353-1365 https://doi.org/10.1016/S1470-2045(20)30445-9
Reference Ris Wihthout Link
- 124
Xavier JB,
Young VB,
Skufca J,
Ginty F,
Testerman T,
Pearson AT.
et al.
The cancer microbiome: distinguishing direct and indirect effects requires a systemic
view. Trends Cancer 2020; Mar; 6 (03) 192-204 https://doi.org/10.1016/j.trecan.2020.01.004
Reference Ris Wihthout Link
- 125
Gopalakrishnan V,
Spencer CN,
Nezi L,
Reuben A,
Andrews MC,
Karpinets TV.
et al.
Gut microbiome modulates response to anti-PD-1 immunotherapy in melanoma patients.
Science 2018; 359 (6371) 97-103 https://doi.org/10.1126/science.aan4236
Reference Ris Wihthout Link
- 126
Matson V,
Fessler J,
Bao R,
Chongsuwat T,
Zha Y,
Alegre ML.
et al.
The commensal microbiome is associated with anti-PD-1 efficacy in metastatic melanoma
patients. Science 2018; 359 (6371) 104-108 https://doi.org/10.1126/science.aao3290
Reference Ris Wihthout Link
- 127
Flanagan L,
Schmid J,
Ebert M,
Soucek P,
Kunicka T,
Liska V.
et al.
Fusobacterium nucleatum associates with stages of colorectal neoplasia development,
colorectal cancer and disease outcome. Eur J Clin Microbiol Infect Dis 2014; Mar;
33: 1381-1390 https://doi.org/10.1007/s10096-014-2081-3
Reference Ris Wihthout Link
- 128
Mima K,
Nishihara R,
Qian ZR,
Cao Y,
Sukawa Y,
Nowak JA.
et al.
Fusobacterium nucleatum in colorectal carcinoma tissue and patient prognosis. Gut
2016; 65 (12) 1973-1980 https://doi.org/10.1136/gutjnl-2015-310101
Reference Ris Wihthout Link
- 129
Chen W,
Liu F,
Ling Z,
Tong X,
Xiang C.
Human intestinal lumen and mucosa-associated microbiota in patients with colorectal
cancer. PLoS One 2012; 7 (06) e39743 https://doi.org/10.1371/journal.pone.0039743
Reference Ris Wihthout Link
- 130
Johnson CH,
Dejea CM,
Edler D,
Hoang LT,
Santidrian AF,
Felding BH.
et al.
Metabolism links bacterial biofilms and colon carcinogenesis. Cell Metab 2015; Jun;
21 (06) 891-897 https://doi.org/10.1016/j.cmet.2015.04.011
Reference Ris Wihthout Link
- 131
Pleguezuelos-Manzano C,
Puschhof J,
Huber RA,
Van Hoeck A,
Wood HM,
Nomburg J.
et al.
Mutational signature in colorectal cancer caused by genotoxic pks+ E. coli. Nature
2020; Feb; 580: 269-273 https://doi.org/10.1038/s41586-020-2080-8
Reference Ris Wihthout Link
- 132
Lee-Six H,
Olafsson S,
Ellis P,
Osborne RJ,
Sanders MA,
Moore L.
et al.
The landscape of somatic mutation in normal colorectal epithelial cells. Nature 2019;
Oct; 574: 532-537 https://doi.org/10.1038/s41586-019-1672-7
Reference Ris Wihthout Link