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Association of MicroRNA-652 Expression with Radiation Response of Colorectal Cancer: A Study from Rectal Cancer Patients in a Swedish Trial of Preoperative Radiotherapy.
Pathak, Surajit; Meng, Wen-Jian; Sriramulu, Sushmitha; Jothimani, Ganesan; Jangamreddy, Jaganmohan Reddy; Banerjee, Antara; Ganesan, Alagu Theivanai; Adell, Gunnar; Zhang, Xueli; Sun-Zhang, Alexander; Zhang, Hong; Sun, Xiao-Feng.
  • Pathak S; Department of Oncology and Department of Biomedical and Clinical Sciences, Linköping University, 581 83 Linköping, Sweden.
  • Meng WJ; Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Chettinad Hospital and Research Institute, Kelambakkam, Chennai, Tamil Nadu - 603103, India.
  • Sriramulu S; Department of Oncology and Department of Biomedical and Clinical Sciences, Linköping University, 581 83 Linköping, Sweden.
  • Jothimani G; Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Sichuan-Chengdu, China.
  • Jangamreddy JR; Department of Medical Biotechnology, Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Chettinad Hospital and Research Institute, Kelambakkam, Chennai, Tamil Nadu - 603103, India.
  • Banerjee A; Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Chettinad Hospital and Research Institute, Kelambakkam, Chennai, Tamil Nadu - 603103, India.
  • Ganesan AT; Department of Oncology and Department of Biomedical and Clinical Sciences, Linköping University, 581 83 Linköping, Sweden.
  • Adell G; Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Chettinad Hospital and Research Institute, Kelambakkam, Chennai, Tamil Nadu - 603103, India.
  • Zhang X; Faculty of Allied Health Sciences, Chettinad Academy of Research and Education, Chettinad Hospital and Research Institute, Kelambakkam, Chennai, Tamil Nadu - 603103, India.
  • Sun-Zhang A; Department of Biotechnology, University College of Engineering, BIT Campus, Anna University, Tiruchirappalli, Tamil Nadu, 620024, India.
  • Zhang H; Department of Oncology and Department of Biomedical and Clinical Sciences, Linköping University, 581 83 Linköping, Sweden.
  • Sun XF; School of Medicine, Department of Medical Sciences, Orebro University, Örebro, Sweden.
Curr Gene Ther ; 23(5): 356-367, 2023.
Article en En | MEDLINE | ID: mdl-37076469
ABSTRACT

BACKGROUND:

Radiotherapy is a standard adjuvant therapy in patients with progressive rectal cancer, but many patients are resistant to radiotherapy, leading to poor prognosis. Our study identified microRNA-652 (miR-652) value on radiotherapy response and outcome in rectal cancer patients.

METHODS:

miR-652 expression was determined by qPCR in primary rectal cancer from 48 patients with and 53 patients without radiotherapy. The association of miR-652 with biological factors and the prognosis was examined. The biological function of miR-652 was identified through TCGA and GEPIA database searches. Two human colon cancer cell lines (HCT116 p53+/+ and p53-/-) were used for in vitro study. The molecular interactions of miR-652 and tumor suppressor genes were studied through a computational approach.

RESULTS:

In RT patients, miR-652 expression was significantly decreased in cancers when compared to non-radiotherapy cases (P = 0.002). High miR-652 expression in non-RT patients was with increased apoptosis marker (P = 0.036), ATM (P = 0.010), and DNp73 expression (P = 0.009). High miR-652 expression was related to worse disease-free survival of non-radiotherapy patients, independent of gender, age, tumor stage, and differentiation (P = 0.028; HR = 7.398, 95% CI 0.217-3.786). The biological functional analysis further identified the prognostic value and potential relationship of miR-652 with apoptosis in rectal cancer. miR-652 expression in cancers was negatively related to WRAP53 expression (P = 0.022). After miR-652 inhibition, the estimation of reactive oxygen species, caspase activity, and apoptosis in HCT116 p53+/+ cells was significantly increased compared with HCT116 p53-/- cells after radiation. The results of the molecular docking analysis show that the miR652-CTNNBL1 and miR652-TP53 were highly stable.

CONCLUSION:

Our findings suggest the potential value of miR-652 expression as a marker for the prediction of radiation response and clinical outcome in rectal cancer patients.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / MicroARNs Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans País como asunto: Europa Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Recto / MicroARNs Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans País como asunto: Europa Idioma: En Año: 2023 Tipo del documento: Article