Murine aldo-keto reductase family 1 subfamily B: Identification of AKR1B8 as an ortholog of human AKR1B10

Amit Joshi, Sandeep Rajput, Chun Wang, Jun Ma, Deliang Cao

Research output: Contribution to journalArticlepeer-review

25 Scopus citations

Abstract

Aldo-keto reductase family 1 member B10 (AKR1B10), overexpressed in multiple human cancers, might be implicated in cancer development and progression via detoxifying cytotoxic carbonyls and regulating fatty acid synthesis. In the present study, we investigated the ortholog of AKR1B10 in mice, an ideal modeling organism greatly contributing to human disease investigations. In the mouse, there are three aldo-keto reductase family 1 subfamily B (AKR1B) members, i.e., AKR1B3, AKR1B7, and AKR1B8. Among them, AKR1B8 has the highest similarity to human AKR1B10 in terms of amino acid sequence, computer-modeled structures, substrate spectra and specificity, and tissue distribution. More importantly, similar to human AKR1B10, mouse AKR1B8 associates with murine acetyl-CoA carboxylase-a and mediates fatty acid synthesis in colon cancer cells. Taken together, our data suggest that murine AKR1B8 is the ortholog of human AKR1B10.

Original languageEnglish
Pages (from-to)1371-1378
Number of pages8
JournalBiological Chemistry
Volume391
Issue number12
DOIs
StatePublished - Dec 2010

Keywords

  • AKR1B8 knockdown
  • Acetyl-CoA carboxylase-α
  • Aldo-keto reductase family 1 member B10 (AKR1B10)
  • Aldo-keto reductase family 1 member B8 (AKR1B8)
  • Mouse ortholog

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