Genomic Profiling of Stage II Colorectal Cancer Identifies Candidate Genes Associated with Recurrence-Free Survival, Tumor Location, and Differentiation Grade
- PMID: 32408300
- PMCID: PMC7592935
- DOI: 10.1159/000507118
Genomic Profiling of Stage II Colorectal Cancer Identifies Candidate Genes Associated with Recurrence-Free Survival, Tumor Location, and Differentiation Grade
Abstract
Background: Identification of high-risk stage II colorectal cancer (CRC) patients, potential candidates for adjuvant chemotherapy, is challenging. Current clinical guidelines rely mainly on histopathological markers with relatively weak prognostic value. This motivates further search for prognostic markers.
Methods: This explorative study aimed to identify potential candidate gene mutations to facilitate differentiation between subgroups of patients with CRC stage II. Panel-based massive parallel sequencing was used to genetically characterize tumor tissues from 85 patients radically operated for CRC stage II, of which 12 developed recurrent cancer during follow-up. Genetic data was compared between patients with or without cancer recurrence, between tumors located in colon and in rectum, and for association with tumor differentiation grade.
Results: Genetic variation in ATM, C11ORF65 was associated with recurrence-free survival. Previous reports regarding the association between BRAF mutation and a higher age at diagnosis, and tumor location in colon were confirmed. APC, BRAF, or KRAS mutation was associated with tumor differentiation grade. Multiple correspondence analyses revealed no obvious clustering of patients with the studied clinical characteristics, indicating that the genetic signatures observed here were unique for each individual.
Conclusions: Taken together, we have demonstrated the utility of panel-based massive parallel sequencing to explore the pathogenesis of CRC stage II. We have identified promising candidate gene mutations associated with cancer recurrence, tumor location, and differentiation grade in patients with CRC stage II, which merit further investigation.
Keywords: APC; ATM; BRAF; Colorectal cancer stage II; Genomic profiling; KRAS.
© 2020 The Author(s). Published by S. Karger AG, Basel.
Conflict of interest statement
The authors have no conflicts of interest to declare.
Figures
Similar articles
-
Relationships among KRAS mutation status, expression of RAS pathway signaling molecules, and clinicopathological features and prognosis of patients with colorectal cancer.World J Gastroenterol. 2019 Feb 21;25(7):808-823. doi: 10.3748/wjg.v25.i7.808. World J Gastroenterol. 2019. PMID: 30809081 Free PMC article.
-
Prognostic relevance of KRAS and BRAF mutations in Japanese patients with colorectal cancer.Int J Clin Oncol. 2013 Dec;18(6):1042-8. doi: 10.1007/s10147-012-0501-x. Epub 2012 Nov 29. Int J Clin Oncol. 2013. PMID: 23188063
-
The prognostic value of KRAS and BRAF in stage I-III colorectal cancer. A systematic review.Ann Ital Chir. 2019;90:127-137. Ann Ital Chir. 2019. PMID: 30739887
-
Prevalence and coexistence of KRAS, BRAF, PIK3CA, NRAS, TP53, and APC mutations in Indian colorectal cancer patients: Next-generation sequencing-based cohort study.Tumour Biol. 2017 Feb;39(2):1010428317692265. doi: 10.1177/1010428317692265. Tumour Biol. 2017. PMID: 28222664
-
PIK3CA mutation and clinicopathological features of colorectal cancer: a systematic review and Meta-Analysis.Acta Oncol. 2020 Jan;59(1):66-74. doi: 10.1080/0284186X.2019.1664764. Epub 2019 Sep 23. Acta Oncol. 2020. PMID: 31545109
Cited by
-
ATM is associated with the prognosis of colorectal cancer: a systematic review.Front Oncol. 2025 Mar 12;15:1470939. doi: 10.3389/fonc.2025.1470939. eCollection 2025. Front Oncol. 2025. PMID: 40144209 Free PMC article.
-
Association of clinical outcomes and the predictive value of T lymphocyte subsets within colorectal cancer patients.Front Surg. 2023 May 3;10:1102545. doi: 10.3389/fsurg.2023.1102545. eCollection 2023. Front Surg. 2023. PMID: 37206348 Free PMC article.
References
-
- WHO and the International Agency for Research on Cancer, Lyon, France: The Globocan Project [accessed January 7, 2019] Available from http://gco.iarc.fr/
-
- Engstrom PF, Arnoletti JP, Benson AB, 3rd, Chen YJ, Choti MA, Cooper HS, et al. NCCN clinical practice guidelines in oncology: colon cancer. J Natl Compr Canc Netw. 2009 Sep;7((8)):778–31. - PubMed
-
- Labianca R, Nordlinger B, Beretta GD, Brouquet A, Cervantes A, Group EGW. Primary colon cancer: ESMO Clinical Practice Guidelines for diagnosis, adjuvant treatment and follow-up. Ann Oncol. 2010 May;21 Suppl 5((Suppl 5)):v70–7. - PubMed
-
- Labianca R, Nordlinger B, Beretta GD, Mosconi S, Mandalà M, Cervantes A, et al. Early colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2013 Oct;24 Suppl 6((Suppl 6)):vi64–72. - PubMed
-
- Böckelman C, Engelmann BE, Kaprio T, Hansen TF, Glimelius B. Risk of recurrence in patients with colon cancer stage II and III: a systematic review and meta-analysis of recent literature. Acta Oncol. 2015 Jan;54((1)):5–16. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous