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Plasma microRNA‐192‐5p can predict the response to neoadjuvant chemotherapy and prognosis in esophageal cancer

Esophageal cancer (EC) is the sixth leading cause of cancer‐related death worldwide. Recently, neoadjuvant chemotherapy (NAC) before curative surgery has become a standard treatment for clinical stage II or III EC patients. Some EC patients receive a complete response (CR) by NAC; thus, curative sur...

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Detalles Bibliográficos
Autores principales: Furuke, Hirotaka, Konishi, Hirotaka, Arita, Tomohiro, Kataoka, Satoshi, Shibamoto, Jun, Takabatake, Kazuya, Takaki, Wataru, Shimizu, Hiroki, Yamamoto, Yusuke, Komatsu, Shuhei, Shiozaki, Atsushi, Fujiwara, Hitoshi, Otsuji, Eigo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067423/
https://www.ncbi.nlm.nih.gov/pubmed/36533956
http://dx.doi.org/10.1111/cas.15703
Descripción
Sumario:Esophageal cancer (EC) is the sixth leading cause of cancer‐related death worldwide. Recently, neoadjuvant chemotherapy (NAC) before curative surgery has become a standard treatment for clinical stage II or III EC patients. Some EC patients receive a complete response (CR) by NAC; thus, curative surgery may be unnecessary for such patients. MicroRNA levels in plasma have the potential to be a predictor of response to NAC. In the present study, we focused on miR‐192‐5p, which is highly expressed in EC tissue. The purpose was to investigate the correlations between levels of plasma miR‐192‐5p and the response to NAC. Furthermore, molecular functions of miR‐192‐5p associated with chemosensitivity were examined using EC cell lines. The levels of miR‐192‐5p in plasma before surgery were evaluated in 113 EC patients. Sixty‐nine patients received NAC. miR‐192‐5p levels in the CR group were significantly higher than in the other groups (p = 0.002). The downregulation of miR‐192‐5p in the EC cell line inhibited sensitivity to cisplatin, and the overexpression of miR‐192‐5p in the EC cell line promoted sensitivity to cisplatin. miR‐192‐5p regulated sensitivity to cisplatin by targeting ERCC3 and ERCC4. Plasma miR‐192‐5p could be used as a predictor of response to chemotherapy and prognosis in EC patients.