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Published on: March 30, 2019
LS-007 inhibits melanoma growth via inducing apoptosis and cell cycle arrest and regulating macrophage polarization
Lijie Yin1, Xinghan Liu1, Jinjin Wu1
1The State Key Laboratory of Pharmaceutical Biotechnology, Division of Immunology, Medical School, Nanjing University.
Abstract:
LS-007, an inhibitor of cyclin-dependent kinase 9 (CDK9), exhibits potential antitumor activity against chronic lymphocytic leukemia and ovarian cancer, but its effect on melanoma and tumor microenvironment (TME) has not been reported yet. This study aimed to investigate the role of LS-007 in B16F10 melanoma and relevant mechanisms. LS-007 significantly inhibited viability and induced apoptosis of B16F10 cells in a dose-dependent manner, which were accompanied with the increased ratio of Bax to Bcl-2 and decreased Mcl-1 mRNA level. Western blot analysis showed that LS-007 increased the expression of cleaved caspase-3 and poly ADP-ribose polymerase (PARP). Furthermore, flow cytometry analysis and qRT-PCR results showed that LS-007 treatment resulted in cell cycle arrest by changing cell cycle-related gene expression. Notably, in vivo evaluation showed that LS-007 significantly decreased the weight and volume of tumor and the expression of Ki67, promoted the expression of iNOS and inhibited the expression of CD206, suggesting that LS-007 might inhibit tumor growth by suppressing polarization of macrophages into tumor-associated macrophages (TAMs) in the TME. The increase in M1/M2 treated with LS-007 detected by flow cytometry hinted that macrophages were polarized towards an antitumor phenotype. In addition, LS-007 induced higher apoptotic rate of B16F10 cells when co-cultured B16F10 with BMDMs. LS-007 has inhibitory effects on B16F10 cells in vivo and in vitro via inducing apoptosis, cell cycle arrest, and changing macrophage function in the TME.
Insights
LS-007, a CDK9 inhibitor, effectively reduced melanoma cell viability and tumor growth. It induced apoptosis, cell cycle arrest, and modulated the tumor microenvironment by altering macrophage polarization.
Area of Science:
- Oncology
- Cancer Biology
- Immunology
Background:
- Cyclin-dependent kinase 9 (CDK9) inhibitors show promise against certain cancers.
- The impact of LS-007 on melanoma and its tumor microenvironment (TME) remains unexplored.
Purpose of the Study:
- To investigate the anti-melanoma effects of LS-007.
- To elucidate the mechanisms underlying LS-007's action in B16F10 melanoma cells and the TME.
Main Methods:
- In vitro studies using B16F10 melanoma cells assessed viability, apoptosis, cell cycle, and gene expression.
- In vivo studies evaluated LS-007's effect on tumor growth, Ki67, iNOS, and CD206 expression.
- Flow cytometry analyzed macrophage polarization (M1/M2 ratio) and apoptosis in co-cultures with bone marrow-derived macrophages (BMDMs).
Main Results:
- LS-007 inhibited B16F10 cell viability and induced apoptosis dose-dependently, increasing Bax/Bcl-2 ratio and decreasing Mcl-1.
- LS-007 caused cell cycle arrest and increased cleaved caspase-3 and PARP expression.
- In vivo, LS-007 reduced tumor weight/volume, Ki67, and CD206, while increasing iNOS, indicating suppressed M2 macrophage polarization and promotion of M1 phenotype.
Conclusions:
- LS-007 demonstrates significant anti-melanoma activity in vitro and in vivo.
- Mechanisms include apoptosis induction, cell cycle arrest, and reprogramming of the TME by shifting macrophage polarization towards an anti-tumor M1 phenotype.
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