2019-nCoV may create complications in colon cancer patients with ACE2 expression

Yongyi Chen1,2,3, Wangang Gong1,2,3, Haibin Wei1,2,3

  • 1Institute of Cancer Research and Basic Medical Sciences, Chinese Academy of Sciences Hangzhou 310022, China.

Insights

The novel coronavirus (2019-nCoV) may pose increased risks for colon cancer patients. This is because ACE2, a key viral entry receptor, is highly expressed in colon tumors, potentially increasing complications.

Area of Science:

  • Virology
  • Oncology
  • Gastroenterology

Background:

  • A novel coronavirus (2019-nCoV) emerged in late 2019, with its full impact on various patient groups still under investigation.
  • Angiotensin-converting enzyme II (ACE2) is identified as the primary cell receptor for 2019-nCoV entry into host cells, mirroring the mechanism of SARS coronavirus.
  • ACE2 expression is notably high in the gastrointestinal tract, particularly in the colon.

Purpose of the Study:

  • To investigate the potential risks and complications of 2019-nCoV infection in patients with colon cancer.
  • To explore the correlation between ACE2 expression and colon cancer, considering its role in viral entry.

Main Methods:

  • Review of existing literature on 2019-nCoV, ACE2, and SARS coronavirus.
  • Analysis of gene expression data, specifically focusing on ACE2, TMPRSS2, and AAK1 in colon tissues.
  • Utilizing the Database of Gene expression profiling interactive analysis (GEPIA).

Main Results:

  • ACE2 expression is significantly elevated in colon cancer tissues compared to other cancer types.
  • ACE2, TMPRSS2, and AAK1 (involved in viral entry and endocytosis) show positive correlation in colon cells.
  • This suggests a potential mechanism for increased viral entry and complications in colon cancer patients.

Conclusions:

  • The heightened expression of ACE2 and associated proteins in colon cancer tissues suggests a higher susceptibility to 2019-nCoV infection.
  • Colon cancer patients may face increased complications due to the viral entry mechanism facilitated by ACE2, TMPRSS2, and AAK1.
  • Further research is warranted to confirm these predictions and develop targeted strategies for managing 2019-nCoV in this vulnerable population.

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