PMID- 29135090 OWN - NLM STAT- MEDLINE DCOM- 20190814 LR - 20190814 IS - 1107-0625 (Print) IS - 1107-0625 (Linking) VI - 22 IP - 5 DP - 2017 Sep-Oct TI - Gene expression profiling demonstrates WNT/beta-catenin pathway genes alteration in Mexican patients with colorectal cancer and diabetes mellitus. PG - 1107-1114 AB - PURPOSE: Several studies have shown a strong association between diabetes mellitus (DM) and increased risk of colorectal cancer (CRC). The fundamental mechanisms that support this association are not entirely understood; however, it is believed that hyperinsulinemia and hyperglycemia may be involved. Some proposed mechanisms include upregulation of mitogenic signaling pathways like MAPK, PI3K, mTOR, and WNT, which are involved in cell proliferation, growth, and cancer cell survival. The purpose of this study was to evaluate the gene expression profile and identify differently expressed genes involved in mitogenic pathways in CRC patients with and without DM. METHODS: In this study, microarray analysis of gene expression followed by quantitative PCR (qPCR) was performed in cancer tissue from CRC patients with and without DM to identify the gene expression profiles and validate the differently expressed genes. RESULTS: Among the study groups, some differently expressed genes were identified. However, when bioinformatics clustering tools were used, a significant modulation of genes involved in the WNT pathway was evident. Therefore, we focused on genes participating in this pathway, such as WNT3A, LRP6, TCF7L2, and FRA-1. Validation of the expression levels of those genes by qPCR showed that CRC patients without type 2 diabetes mellitus (T2DM) expressed significantly more WNT3Ay LRP6, but less TCF7L2 and FRA-1 compared to controls, while in CRC patients with DM the expression levels of WNT3A, LRP6, TCF7L2, and FRA-1 were significantly higher compared to controls. CONCLUSIONS: Our results suggest that WNT/beta-catenin pathway is upregulated in patients with CRC and DM, demonstrating its importance and involvement in both pathologies. FAU - Ivonne Wence-Chavez, Laura AU - Ivonne Wence-Chavez L AD - Doctorate Program in Molecular Biology, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico. FAU - Palomares-Chacon, Ulises AU - Palomares-Chacon U FAU - Pablo Flores-Gutierrez, Juan AU - Pablo Flores-Gutierrez J FAU - Felipe Jave-Suarez, Luis AU - Felipe Jave-Suarez L FAU - Del Carmen Aguilar-Lemarroy, Adriana AU - Del Carmen Aguilar-Lemarroy A FAU - Barros-Nunez, Patricio AU - Barros-Nunez P FAU - Esperanza Flores-Martinez, Silvia AU - Esperanza Flores-Martinez S FAU - Sanchez-Corona, Jose AU - Sanchez-Corona J FAU - Alejandra Rosales-Reynoso, Monica AU - Alejandra Rosales-Reynoso M LA - eng PT - Journal Article PL - Cyprus TA - J BUON JT - Journal of B.U.ON. : official journal of the Balkan Union of Oncology JID - 100883428 RN - 0 (beta Catenin) MH - Aged MH - Colorectal Neoplasms/*genetics/pathology MH - Diabetes Mellitus, Type 2/*genetics/pathology MH - Female MH - Gene Expression Profiling/methods MH - Humans MH - Male MH - Mexico MH - Middle Aged MH - Wnt Signaling Pathway/*physiology MH - beta Catenin/*genetics EDAT- 2017/11/15 06:00 MHDA- 2019/08/15 06:00 CRDT- 2017/11/15 06:00 PHST- 2017/11/15 06:00 [entrez] PHST- 2017/11/15 06:00 [pubmed] PHST- 2019/08/15 06:00 [medline] PST - ppublish SO - J BUON. 2017 Sep-Oct;22(5):1107-1114.