Downregulation of miR-301a-3p sensitizes pancreatic cancer cells to gemcitabine treatment via PTEN.

Xiang Xia(Shanghai First People's Hospital), Kundong Zhang(Shanghai First People's Hospital), Guangtao Luo(Shanghai First People's Hospital), Gang Cen(Shanghai First People's Hospital), Jun Cao(Shanghai First People's Hospital), Kejian Huang(Shanghai First People's Hospital), Zhengjun Qiu(Shanghai First People's Hospital)
PubMed
January 1, 2017
Cited by 52Open Access

Abstract

BACKGROUND: We previously showed that miR-301a-3p affects the invasion and migration abilities of pancreatic cancer cells. Here, we explore the role of miR-301a-3p in chemoresistance, which represents a major obstacle in cancer treatment. METHODS: . We used quantitative real-time PCR (qRT-PCR) to measure miR-301a-3p expression in wild-type and gemcitabine-resistant pancreatic cancer cells. We performed Western blot, qRT-PCR, and luciferase and rescue assays to confirm the direct target of miR-301a-3p. RESULTS: . The role of miR-301-3p in chemoresistance was dependent on PTEN. The suppression of miR-301-3p expression sensitized pancreatic cancer cells to gemcitabine chemotherapy in a xenograft mouse model. CONCLUSION: MiR-301a-3p confers resistance to gemcitabine by regulating the expression of PTEN. The co-delivery of miR-301a-3p and gemcitabine might be an effective therapeutic regimen for patients with pancreatic cancer.


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