Overexpression of microRNA-130a predicts adverse prognosis of primary gastrointestinal diffuse large B-cell lymphoma
Autor: | Yong Yu, Peng Ge, Yafei Wang, Haifeng Zhao, Xianming Liu, Hongliang Yang, Xinyuan Wang, Lanfang Li, Zhigang Zhao, Yutian Kan, Xiaofang Wang, Zhengzi Qian, Qiongli Zhai, Lihua Qiu, Leiyuan Chen, Huilai Zhang, Tingting Ding |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Oncology Cancer Research medicine.medical_specialty microRNA-130a resistance 03 medical and health sciences 0302 clinical medicine International Prognostic Index Internal medicine hemic and lymphatic diseases expression medicine Neprilysin Survival analysis Proportional hazards model business.industry Hazard ratio Cancer primary gastrointestinal diffuse large B-cell lymphoma Articles medicine.disease Lymphoma 030104 developmental biology 030220 oncology & carcinogenesis prognosis business Diffuse large B-cell lymphoma |
Zdroj: | Oncology Letters |
ISSN: | 1792-1082 1792-1074 |
Popis: | Primary gastrointestinal diffuse large B-cell lymphoma (PGI-DLBCL) is a highly heterogeneous type of non-Hodgkin lymphoma. A number of studies have demonstrated that microRNA-130a (miR-130a) serves a role in the tumorigenesis and prognosis of numerous human tumors. However, to the best of our knowledge, the prognostic significance of miR-130a in PGI-DLBCL remains unknown. The present study explored the association between miR-130a and the clinical outcomes of PGI-DLBCL. Relative miR-130a expression was assessed by reverse transcription-quantitative PCR. Immunohistochemistry was used to detect expression levels of BCL-2, c-MYC, neprilysin, B-cell lymphoma 6 protein, PWWP domain-containing DNA repair factor 3A and proliferation marker protein Ki-67. A receiver operating characteristic curve was constructed to analyze the specificity and sensitivity of microRNA levels in the diagnosis of PGI-DLBCL. Survival curves were constructed using the Kaplan-Meier method. In the present study, miR-130a expression was notably higher in patients with PGI-DLBCL compared with in the controls (P |
Databáze: | OpenAIRE |
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