MiR-3619-5p hampers proliferation and cisplatin resistance in cutaneous squamous-cell carcinoma via KPNA4

被引:41
作者
Zhang, Mingfeng [1 ]
Luo, Heng [2 ]
Hui, Li [3 ]
机构
[1] Huzhou Hosp Tradit Chinese Med, Dept Dermatol, Huzhou 313000, Zhejiang, Peoples R China
[2] Tongji Univ, Shanghai Pulm Hosp, Dept Pharm, Sch Med, Shanghai 200433, Peoples R China
[3] Yanan Univ, Dept Pharm, Affiliated Hosp, Yanan 716000, Shaanxi, Peoples R China
关键词
CSCC; miR-3619-5p; Cisplatin resistance; KPNA4; BREAST-CANCER; SKIN-CANCER; INHIBITION; CHEMORESISTANCE; APOPTOSIS; MECHANISM; GROWTH;
D O I
10.1016/j.bbrc.2019.03.203
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cutaneous squamous cell carcinoma (CSCC) remains the second most prevailing cancer worldwide and presents high mortality rates. Given that chemoresistance becomes an enormous obstacle to the therapy for CSCC patients, there is a pressing need to discover novel strategies for enhancing the response of CSCC cells to cisplatin. Emerging evidence has unfolded that miRNAs are participated in regulation of drug resistance in multiple cancers. MiR-3619-5p has been proofed to exert tumor inhibitive activities in human malignancies, but the biological function of miR-3619-5p in the progression of CSCC is still unclear. In this study, we observed that miR-3619-5p expression was pronouncedly dropped in cisplatin-resistant CSCC cells. Subsequently, miR-3619-5p was validated to act as a tumor suppressor in CSCC through retarding cell proliferation and cisplatin resistance. Besides, our findings certified that KPNA4 was highly expressed in cisplatin-resistant CSCC cells. Further, KPNA4 was negatively regulated by miR-3619-5p. Rescue experiments unveiled that KPNA4 counteracted the miR-3619-5p-mediated regulation of CSCC tumorigenesis. On the whole, miR-3619-5p inhibited cell proliferation and cisplatin resistance of CSCC by regulating KPNA4 expression, suggesting that miR-3619-5p/KPNA4 pathway may represent a potential promising strategy for the treatment of patients with CSCC. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:419 / 425
页数:7
相关论文
共 35 条
[1]   Primary care: Cutaneous squamous-cell carcinoma [J].
Alam, M ;
Ratner, D .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (13) :975-983
[2]  
Ayers D., 2017, GENES, P8
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   MicroRNA-567 dysregulation contributes to carcinogenesis of breast cancer, targeting tumor cell proliferation, and migration [J].
Bertoli, Gloria ;
Cava, Claudia ;
Diceglie, Cecilia ;
Martelli, Cristina ;
Rizzo, Giampiero ;
Piccotti, Francesca ;
Ottobrini, Luisa ;
Castiglioni, Isabella .
BREAST CANCER RESEARCH AND TREATMENT, 2017, 161 (03) :605-616
[5]   Contribution of FPR and TLR9 to hypoxia-induced chemoresistance of ovarian cancer cells [J].
Cai, Yongqing ;
Huang, Jian ;
Xing, Haiyan ;
Li, Bin ;
Li, Ling ;
Wang, Xianfeng ;
Peng, Dan ;
Chen, Jianhong .
ONCOTARGETS AND THERAPY, 2019, 12 :291-301
[6]   Concomitant inhibition of AKT and autophagy is required for efficient cisplatin-induced apoptosis of metastatic skin carcinoma [J].
Claerhout, Sofie ;
Verschooten, Lien ;
Van Kelst, Sofie ;
De Vos, Rita ;
Proby, Charlotte ;
Agostinis, Patrizia ;
Garmyn, Marjan .
INTERNATIONAL JOURNAL OF CANCER, 2010, 127 (12) :2790-2803
[7]   Chemotherapy of Squamous Cell Carcinoma of the Skin [J].
DeConti, Ronald C. .
SEMINARS IN ONCOLOGY, 2012, 39 (02) :145-149
[8]   Nonmelanoma Skin Cancer [J].
Dubas, Lauren E. ;
Ingraffea, Adam .
FACIAL PLASTIC SURGERY CLINICS OF NORTH AMERICA, 2013, 21 (01) :43-+
[9]   NF-κB is transported into the nucleus by importin α3 and importin α4 [J].
Fagerlund, R ;
Kinnunen, L ;
Köhler, M ;
Julkunen, I ;
Melén, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (16) :15942-15951
[10]  
Garcia-Zuazaga Jorge, 2008, Adv Dermatol, V24, P33, DOI 10.1016/j.yadr.2008.09.007