STAT1 is a sex-specific tumor suppressor in colitis-associated colorectal cancer

Abstract

The interferon-inducible transcription factor STAT1 is a tumor suppressor in various malignancies. We investigated sex-specific STAT1 functions in colitis and colitis-associated colorectal cancer (CRC) using mice with specific STAT1 deletion in intestinal epithelial cells (STAT1^∆IEC ). Male but not female STAT1^∆IEC mice were more resistant to DSS-induced colitis than sex-matched STAT1^flox/flox controls and displayed reduced intraepithelial infiltration of CD8⁺ TCRαβ⁺ granzyme B⁺ T cells. Moreover, DSS treatment failed to induce expression of T-cell-attracting chemokines in intestinal epithelial cells of male but not of female STAT1^∆IEC mice. Application of the AOM-DSS protocol for induction of colitis-associated CRC resulted in increased intestinal tumor load in male but not in female STAT1^∆IEC mice. A sex-specific stratification of human CRC patients corroborated the data obtained in mice and revealed that reduced tumor cell-intrinsic nuclear STAT1 protein expression is a poor prognostic factor in men but not in women. These data demonstrate that epithelial STAT1 is a male-specific tumor suppressor in CRC of mice and humans.

Keywords: CD8+ T cells; STAT1; colitis; colorectal cancer; gender; sex.