Background: - Colorectal cancer (CRC) is a common worldwide cancer and
the fourth worldwide cause of cancer death. Autophagy has been highlighted as a
promising molecular target in cancer. Its role in carcinogenesis is complex
with a reported oncogenic or tumor suppressive role. Detecting LC3 has become a
reliable method for monitoring autophagy. Signal transducers and activators of
transcription (STAT) proteins are latent cytoplasmic transcription factors.
MicroRNAs (miRNAs) are small non-coding RNAs which post-transcriptionally
regulate gene expression. Aim:- To search for the expression of LC3, as a
marker of autophagy, STAT3 and miRNA 101 as possible regulators of autophagy
and/ or potential molecular prognostic targets in Egyptian CRC patients.
Material and methods:- Twenty five CRC and 25 adjacent normal mucosa specimens
were obtained. Immunohistochemical assessment of LC3 expression using anti-LC3
and assessment of STAT3 and microRNA 101 expressions by real time - RT - PCR
were done. Results: - Revealed a statistically significant increase in LC3
(p<0.001) and STAT3 expression in tumor samples (6.31 ± 1.96 folds) than
normal mucosa (p<0.001 each). Both of them were directly correlated together
(r= 0.833, p <0.001). MicroRNA 101 was inversely correlated to both LC3 and
STAT3 (p<0.001) and was significantly reduced in tumor samples (0.37 ± 0.16
folds) (p<0.001) with a possible correlations to tumor characteristics.
Conclusion:- LC3, STAT3 and miRNA 101 may be valuable as biomarkers that may
predict cancer colon poor prognosis. The critical role of STAT3 and miRNAs in
autophagy would expand our knowledge of the molecular mechanisms of autophagy
regulation. - See more at: .
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