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人成纤维细胞中激活转录因子3的上调通过旁分泌途径抑制黑色素瘤细胞的生长和迁移。

Up-Regulation of Activating Transcription Factor 3 in Human Fibroblasts Inhibits Melanoma Cell Growth and Migration Through a Paracrine Pathway.

作者信息

Zu Tingjian, Wen Jie, Xu Lin, Li Hui, Mi Jun, Li Hui, Brakebusch Cord, Fisher David E, Wu Xunwei

机构信息

Department of Tissue Engineering and Regeneration, School and Hospital of Stomatology, Shandong University, Jinan, China.

Shandong Key Laboratory of Oral Tissue Regeneration and Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, Jinan, China.

出版信息

Front Oncol. 2020 Apr 21;10:624. doi: 10.3389/fonc.2020.00624. eCollection 2020.

DOI:10.3389/fonc.2020.00624
PMID:32373541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7187895/
Abstract

The treatment of melanoma has remained a difficult challenge. Targeting the tumor stroma has recently attracted attention for developing novel strategies for melanoma therapy. Activating transcription factor 3 (ATF3) plays a crucial role in regulating tumorigenesis and development, but whether the expression of ATF3 in human dermal fibroblasts (HDFs) can affect melanoma development hasn't been studied. Our results show that ATF3 expression is downregulated in stromal cells of human melanoma. HDFs expressing high levels of ATF3 suppressed the growth and migration of melanoma cells in association with downregulation of different cytokines including IL-6 . , HDFs with high ATF3 expression reduced tumor formation. Adding recombinant IL-6 to melanoma cells reversed those and effects, suggesting that ATF3 expression by HDFs regulates melanoma progression through the IL-6/STAT3 pathway. More importantly, HDFs pretreated with cyclosporine A or phenformin to induce ATF3 expression inhibited melanoma cell growth and . In summary, our study reveals that ATF3 suppresses human melanoma growth and that inducing the expression of ATF3 in HDFs can inhibit melanoma growth, a new potential melanoma therapeutic approach.

摘要

黑色素瘤的治疗一直是一项艰巨的挑战。靶向肿瘤基质最近在开发黑色素瘤治疗新策略方面受到关注。激活转录因子3(ATF3)在调节肿瘤发生和发展中起关键作用,但ATF3在人皮肤成纤维细胞(HDFs)中的表达是否会影响黑色素瘤的发展尚未得到研究。我们的结果表明,ATF3在人黑色素瘤基质细胞中的表达下调。高表达ATF3的HDFs与包括IL-6在内的不同细胞因子的下调相关,抑制了黑色素瘤细胞的生长和迁移。 ,高ATF3表达的HDFs减少了肿瘤形成。向黑色素瘤细胞中添加重组IL-6可逆转上述 和 效应,表明HDFs中的ATF3表达通过IL-6/STAT3途径调节黑色素瘤进展。更重要的是,用环孢素A或二甲双胍预处理以诱导ATF3表达的HDFs抑制了黑色素瘤细胞的生长 和 。总之,我们的研究表明ATF3抑制人黑色素瘤生长,并且在HDFs中诱导ATF3表达可以抑制黑色素瘤生长,这是一种新的潜在黑色素瘤治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/fef2b2d24316/fonc-10-00624-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/78dca11a943f/fonc-10-00624-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/478b322a513f/fonc-10-00624-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/cfe6dcef2146/fonc-10-00624-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/0dfd0984ed6a/fonc-10-00624-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/9bd5d7751d1b/fonc-10-00624-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/fef2b2d24316/fonc-10-00624-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/78dca11a943f/fonc-10-00624-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/478b322a513f/fonc-10-00624-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/cfe6dcef2146/fonc-10-00624-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/0dfd0984ed6a/fonc-10-00624-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/9bd5d7751d1b/fonc-10-00624-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/582b/7187895/fef2b2d24316/fonc-10-00624-g0006.jpg

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