Patients with mismatch repair (MMR)-deficient colorectal cancer (CRC) have a more favorable prognosis than patients with tumors with intact MMR. In order to obtain further insights on the reasons for this different outcome, we investigated the interplay between MMR genes and TLR4/MyD88 signaling. The cancer genome atlas (TCGA) databases were selected to predict the differential expression of TLR4 in colon cancer and its correlation with MMR genes. Moreover, the expression of MMR genes and TLR4 was evaluated by immunohistochemistry in 113 CRC samples and a cohort of 63 patients was used to assess mRNA expression and epigenetic silencing status. , the effect of knockdown on expression was quantified by Real Time PCR. TLR4 expression resulted dependent on MMR status and directly correlated to MLH1 expression. , silencing decreased expression. These observations may reflect the better prognosis and the chemoresistance of patients with CRC and MMR defects.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8139190 | PMC |
http://dx.doi.org/10.3389/fmolb.2021.624873 | DOI Listing |
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