Molecular and phenotypic profiling of colorectal cancer patients in West Africa reveals biological insights Journal Article


Authors: Alatise, O. I.; Knapp, G. C.; Sharma, A.; Chatila, W. K.; Arowolo, O. A.; Olasehinde, O.; Famurewa, O. C.; Omisore, A. D.; Komolafe, A. O.; Olaofe, O. O.; Katung, A. I.; Ibikunle, D. E.; Egberongbe, A. A.; Olatoke, S. A.; Agodirin, S. O.; Adesiyun, O. A.; Adeyeye, A.; Kolawole, O. A.; Olakanmi, A. O.; Arora, K.; Constable, J.; Shah, R.; Basunia, A.; Sylvester, B.; Wu, C.; Weiser, M. R.; Seier, K.; Gonen, M.; Stadler, Z. K.; Kemel, Y.; Vakiani, E.; Berger, M. F.; Chan, T. A.; Solit, D. B.; Shia, J.; Sanchez-Vega, F.; Schultz, N.; Brennan, M.; Smith, J. J.; Kingham, T. P.
Article Title: Molecular and phenotypic profiling of colorectal cancer patients in West Africa reveals biological insights
Abstract: Understanding the molecular and phenotypic profile of colorectal cancer (CRC) in West Africa is vital to addressing the regions rising burden of disease. Tissue from unselected Nigerian patients was analyzed with a multigene, next-generation sequencing assay. The rate of microsatellite instability is significantly higher among Nigerian CRC patients (28.1%) than patients from The Cancer Genome Atlas (TCGA, 14.2%) and Memorial Sloan Kettering Cancer Center (MSKCC, 8.5%, P < 0.001). In microsatellite-stable cases, tumors from Nigerian patients are less likely to have APC mutations (39.1% vs. 76.0% MSKCC P < 0.001) and WNT pathway alterations (47.8% vs. 81.9% MSKCC, P < 0.001); whereas RAS pathway alteration is more prevalent (76.1% vs. 59.6%, P = 0.03). Nigerian CRC patients are also younger and more likely to present with rectal disease (50.8% vs. 33.7% MSKCC, P < 0.001). The findings suggest a unique biology of CRC in Nigeria, which emphasizes the need for regional data to guide diagnostic and treatment approaches for patients in West Africa. © 2021, The Author(s).
Keywords: biology; molecular analysis; disease treatment; nigeria; disease prevalence; cancer; biological method
Journal Title: Nature Communications
Volume: 12
ISSN: 2041-1723
Publisher: Nature Publishing Group  
Date Published: 2021-11-24
Start Page: 6821
Language: English
DOI: 10.1038/s41467-021-27106-w
PROVIDER: scopus
PMCID: PMC8613248
PUBMED: 34819518
DOI/URL:
Notes: Article -- Export Date: 3 January 2022 -- Source: Scopus
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MSK Authors
  1. Timothy Chan
    317 Chan
  2. Murray F Brennan
    1059 Brennan
  3. David Solit
    781 Solit
  4. Mithat Gonen
    1032 Gonen
  5. Zsofia Kinga Stadler
    393 Stadler
  6. Jinru Shia
    720 Shia
  7. Martin R Weiser
    540 Weiser
  8. T Peter Kingham
    618 Kingham
  9. Michael Forman Berger
    768 Berger
  10. Efsevia Vakiani
    265 Vakiani
  11. Nikolaus D Schultz
    491 Schultz
  12. Yelena Kemel
    104 Kemel
  13. Ronak Hasmukh Shah
    72 Shah
  14. Jesse Joshua Smith
    227 Smith
  15. Kenneth Seier
    108 Seier
  16. Walid Khaled Chatila
    104 Chatila
  17. Chao Wu
    21 Wu
  18. Gregory Christopher Knapp
    7 Knapp
  19. Avinash Sunil Sharma
    15 Sharma
  20. Kanika Suresh Arora
    27 Arora