Literature DB >> 26700670

MicroRNA-148a represents an independent prognostic marker in bladder cancer.

Lin Ma1, Zhishun Xu1, Chao Xu2, Xianzhou Jiang3.   

Abstract

A previous study has demonstrated the roles of microRNA-148a (miR-148a) on apoptosis of bladder cancer cells. The goal of this study was to investigate whether the miR-148a expression level could serve as a new biomarker for the prognosis of bladder cancer patients. We collected a total of 126 bladder cancer samples. The expression level of miR-148a was determined with quantitative real-time polymerase chain reaction (qRT-PCR). Kaplan-Meier method was used to analyze the overall survival. Cox regression analysis was further used to identify prognostic factors. The expression levels of miR-148a in bladder cancer tissues were identified (1.5 ± 0.3; P < 0.001). The bladder cancer patients in the low-expression group more frequently had a high tumor grade (P = 0.025), increased tumor recurrence (P = 0.002), and advanced lymph node (LN) metastasis (P = 0.001). Patient survival analysis revealed a clear positive correlation between miR-148a expression level and survival time of bladder cancer patients (P = 0.005, log-rank = 7.714). In univariate Cox proportional hazards regression analysis, we found that a low-expression level of miR-148a (P = 0.018), tumor grade (P = 0.006), lymph node metastasis (P = 0.001), and recurrence (P < 0.001) were associated with the prognosis of bladder cancer. In multivariate analysis, we found that miR-148a expression (RR = 0.206, 95 % CI 0.095-0.813, P = 0.029), tumor grade (RR = 0.714, 95 % CI 0.224-0.958, P = 0.714), lymph node metastasis (RR = 6.604, 95 % CI 3.192-12.547, P < 0.001), and recurrence (RR = 15.126, 95 % CI 6.714-22.025, P < 0.001) retained significance as an independent prognostic factor of bladder cancer survival (Table 3). All results have showed that miR-148a expression was decreased in bladder cancer specimens and reduced miR-148a expression was associated with poorer survival time, indicating that miR-148a may become a candidate factor for predicting the prognosis of bladder cancer.

Entities:  

Keywords:  Bladder cancer; Prognosis; Survival; miR-148a

Mesh:

Substances:

Year:  2015        PMID: 26700670     DOI: 10.1007/s13277-015-4688-0

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  38 in total

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5.  MicroRNA-101 is down-regulated in gastric cancer and involved in cell migration and invasion.

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Review 7.  MicroRNAs: new tools for diagnosis, prognosis, and therapy in hepatocellular carcinoma?

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Journal:  Hepatology       Date:  2012-12-26       Impact factor: 17.425

8.  Recurrence of early stage colon cancer predicted by expression pattern of circulating microRNAs.

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Journal:  J Biomed Res       Date:  2011-05
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1.  Depletion of tumor suppressor miRNA-148a in plasma relates to tumor progression and poor outcomes in gastric cancer.

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Journal:  Am J Cancer Res       Date:  2021-12-15       Impact factor: 6.166

2.  miR-148a-3p represses proliferation and EMT by establishing regulatory circuits between ERBB3/AKT2/c-myc and DNMT1 in bladder cancer.

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Review 4.  Dysregulation of miRNAs in bladder cancer: altered expression with aberrant biogenesis procedure.

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Journal:  Oncotarget       Date:  2017-04-18

Review 5.  Emerging Biomarkers for Predicting Bladder Cancer Lymph Node Metastasis.

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6.  miR-148a-3p inhibits the proliferation and migration of bladder cancer via regulating the expression of ROCK-1.

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Journal:  PeerJ       Date:  2022-01-26       Impact factor: 2.984

7.  miRNA-148a and miRNA-30c expressions as potential biomarkers in breast cancer patients.

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8.  miR-148a and miR-375 may serve as predictive biomarkers for early diagnosis of laryngeal carcinoma.

Authors:  Ying Wu; Jia Yu; Yanni Ma; Fang Wang; Honggang Liu
Journal:  Oncol Lett       Date:  2016-06-13       Impact factor: 2.967

9.  Evaluating the prognostic value of miR-148/152 family in cancers: based on a systemic review of observational studies.

Authors:  Fujiao Duan; Weigang Liu; Xiaoli Fu; Yajing Feng; Liping Dai; Shuli Cui; Zhenxing Yang
Journal:  Oncotarget       Date:  2017-09-11
  9 in total

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