Literature DB >> 34628519

Down-regulated expression of miR-582 predicts poor prognosis and facilitates melanoma progression by targeting FOXC1.

Fang Chen1, Dapeng Zhang2.   

Abstract

Melanoma is one of the most common malignant tumors that originate from nerve sheath melanocytes and are produced in the skin and other organs. This paper mainly studied the role of miR-582 in melanoma. The expression of miR-582 in melanoma cell lines and tissues was evaluated by real-time quantitative PCR. Kaplan-Meier curve and Cox proportional hazards model analysis were used to investigate the prognostic value of miR-582 in melanoma. Cell proliferation, invasion, and migration were analyzed using CCK-8 and transwell assays. The results showed that miR-582 was significantly decreased in melanoma cells and tissues. Downregulation of miR-582 was associated with ulceration, lymph node metastasis, TNM stage, and poor overall survival. The functional results showed that low expression of miR-582 can promote cell proliferation, migration, and invasion. FOXC1 was a direct target of miR-582. Overall, the expression of miR-582 is downregulated in melanoma tissues and cell lines. Low expression of miR-582 is associated with prognosis and progression of melanoma by targeting FOXC1. miR-582 may be a prognostic biomarker and a new therapeutic strategy for melanoma.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  FOXC1; Invasion; Melanoma; Migration; miR-582

Mesh:

Substances:

Year:  2021        PMID: 34628519     DOI: 10.1007/s00403-021-02285-0

Source DB:  PubMed          Journal:  Arch Dermatol Res        ISSN: 0340-3696            Impact factor:   3.033


  32 in total

1.  Melanoma diagnosis: predictive value of macroscopic changes observed by the patient.

Authors:  Isabelle Tromme; Laurine Sacré; Fatima Hammouch; Pauline Richez; Jean-Marie Degryse; Niko Speybroeck
Journal:  Melanoma Res       Date:  2018-12       Impact factor: 3.599

Review 2.  Novel approaches in melanoma prevention and therapy.

Authors:  Antonio M Grimaldi; Pamela B Cassidy; Sancy Leachmann; Paolo A Ascierto
Journal:  Cancer Treat Res       Date:  2014

Review 3.  Malignant melanoma.

Authors:  A Slominski; J Wortsman; A J Carlson; L Y Matsuoka; C M Balch; M C Mihm
Journal:  Arch Pathol Lab Med       Date:  2001-10       Impact factor: 5.534

Review 4.  Melanoma Development: Current Knowledge on Melanoma Pathogenesis.

Authors:  Liborija Lugović-Mihić; Diana Ćesić; Petra Vuković; Gaby Novak Bilić; Mirna Šitum; Sanja Špoljar
Journal:  Acta Dermatovenerol Croat       Date:  2019-09       Impact factor: 1.256

Review 5.  Immunotherapy of Melanoma.

Authors:  Carolin Bender; Jessica C Hassel; Alexander Enk
Journal:  Oncol Res Treat       Date:  2016-05-25       Impact factor: 2.825

6.  Identification of epigenetically altered genes and potential gene targets in melanoma using bioinformatic methods.

Authors:  Honghao Duan; Ke Jiang; Dengke Wei; Lijun Zhang; Deliang Cheng; Min Lv; Yuben Xu; Aimin He
Journal:  Onco Targets Ther       Date:  2017-12-20       Impact factor: 4.147

7.  MicroRNA-338-3p suppresses cell proliferation, migration and invasion in human malignant melanoma by targeting MACC1.

Authors:  Chunhua Zhang; Hui Li; Junling Wang; Jibei Zhang; Xiaoqian Hou
Journal:  Exp Ther Med       Date:  2019-06-04       Impact factor: 2.447

8.  Profiling of prognostic alternative splicing in melanoma.

Authors:  Fu-Chao Ma; Rong-Quan He; Peng Lin; Jin-Cai Zhong; Jie Ma; Hong Yang; Xiao-Hua Hu; Gang Chen
Journal:  Oncol Lett       Date:  2019-06-07       Impact factor: 2.967

9.  miR-124 Functions As A Melanoma Tumor Suppressor By Targeting RACK1.

Authors:  Congcong Shen; Hui Hua; Lixiong Gu; Shuanglin Cao; Hengji Cai; Xiaodong Yao; Xiaodong Chen
Journal:  Onco Targets Ther       Date:  2019-11-19       Impact factor: 4.147

10.  Genetics and epigenetics of melanoma.

Authors:  Xiao-Ying Zhang; Pei-Ying Zhang
Journal:  Oncol Lett       Date:  2020-09-01       Impact factor: 2.967

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.