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miR-17–92 cluster is connected with disease progression and oxaliplatin/capecitabine chemotherapy efficacy in advanced gastric cancer patients: A preliminary study

This study aimed to determine the role of plasma miR-17–92 cluster level in predicting chemoresistance in patients with gastric cancer (GC) undergoing oxaliplatin/capecitabine (XELOX) chemotherapy. Patients recently diagnosed with advanced GC were chosen as participants based on the inclusion criter...

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Detalles Bibliográficos
Autores principales: Fan, Baohua, Shen, Cunfang, Wu, Milu, Zhao, Junhui, Guo, Qijing, Luo, Yushuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392796/
https://www.ncbi.nlm.nih.gov/pubmed/30170406
http://dx.doi.org/10.1097/MD.0000000000012007
Descripción
Sumario:This study aimed to determine the role of plasma miR-17–92 cluster level in predicting chemoresistance in patients with gastric cancer (GC) undergoing oxaliplatin/capecitabine (XELOX) chemotherapy. Patients recently diagnosed with advanced GC were chosen as participants based on the inclusion criteria. The plasma levels of miR-17-5p, miR-18a, miR-19a/b, miR-20a, and miR-92-1 (miR-17–92 cluster) were determined through quantitative RT-PCR of blood samples from GC patients and healthy volunteers. All the patients received XELOX chemotherapy, and the effectiveness of the chemotherapy was evaluated. The miR-17–92 plasma level was increased in advanced GC patients and decreased after XELOX chemotherapy. Moreover, the miR-17–92 cluster level was associated with chemotherapy response but not with chemotherapy-related toxicity. The miR-17–92 cluster plasma level was decreased in chemosensitive patients, but not in chemoresistant patients, after chemotherapy. The sensitivity and specificity of the combined detection of the miR-17–92 cluster in patients with advanced GC were 100% each. The results suggest that the miR-17–92 plasma level is associated with the progression of advanced GC and effectiveness of XELOX chemotherapy.