Limb-bud and Heart Overexpression Inhibits the Proliferation and Migration of PC3M Cells
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Updated: Feb 15, 2026

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Qicai Liu1,2, Ermao Li3,4, Long Huang3
1Guangdong Provincial Biomedical Engineering Technology Research Center for Cardiovascular Disease; Sino-Japanese Cooperation Platform for Translational Research in Heart Failure; Laboratory of Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou 510280, China.
Insights
Limb-bud and heart gene (LBH) is down-regulated in prostate cancer (PCa). Overexpressing LBH inhibits PCa cell proliferation and tumor growth by causing cell cycle arrest, suggesting LBH as a potential therapeutic target for PCa.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Limb-bud and heart gene (LBH) plays roles in embryonic development and cancer.
- Its specific function in prostate cancer (PCa) remains largely uncharacterized.
- This study investigates LBH's role in PCa cell proliferation and migration.
Purpose of the Study:
- To investigate the expression of LBH in PCa.
- To determine the effect of LBH overexpression on PCa cell behavior.
- To explore LBH as a potential therapeutic target for PCa.
Main Methods:
- Immunohistochemistry and Western blotting to detect LBH expression.
- Lentiviral vectors to overexpress LBH in PC3M cells.
- MTT assay, flow cytometry, and Transwell assay to assess proliferation, cell cycle, apoptosis, and migration.
Main Results:
- LBH expression is downregulated in PCa cell lines, particularly PC3M.
- LBH overexpression in PC3M cells inhibited proliferation and tumor growth in vivo.
- LBH overexpression induced G0/G1 phase cell cycle arrest and reduced cell migration, associated with decreased cyclin D1 and E2 levels.
Conclusions:
- LBH expression is significantly reduced in PCa tissues and cell lines.
- Overexpression of LBH suppresses PCa cell proliferation and tumor growth.
- LBH acts by inducing cell cycle arrest via downregulation of cyclin D1 and E2, positioning it as a potential therapeutic target and diagnostic marker for PCa.
Abstract:
Background: The limb-bud and heart gene (LBH) was discovered in the early 21st century and is specifically expressed in the mouse embryonic limb and heart development. Increasing evidences have indicated that LBH not only plays an important role in embryo development, it is also closely correlated with the occurance and progression of many tumors. However, its function in prostate cancer (PCa) is still not well understood. Here, we explored the effects of LBH on the proliferation and migration of the PCa cell line PC3M. Methods: LBH expression in tissues and cell lines of PCa was detected by immunohistochemistry and Western blotting. Lentivirus was used to transduct the LBH gene into the PC3M cells. Stable LBH-overexpressing PC3M-LBH cells and PC3M-NC control cells were obtained via puromycin screening. Cell proliferation was examined using the 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. Cell cycle distribution and apoptosis rate were investigated using flow cytometry. Cell migration was studied using the Transwell assay. Results: LBH expression level was down-regulated in 3 different PCa cell lines, especially in PC3M cells, compared with the normal prostate epithelial cells(RWPE-1). Cell lines of LBH-upregulated PC3M-LBH and PC3M-NC control were successfully constructed. Significantly increased LBH expression level and decreased cyclin D1 and cyclin E2 expression level was found in PC3M-LBH cells as compared to the PC3M-NC cells. The overexpression of LBH significantly inhibited PC3M cell proliferation in vitro and tumor growth in nude mice. LBH overexpression in PC3M cell, also induced cell cycle G0/G1 phase arrest and decreased the migration of PC3M cells. Conclusions: Our results reveal that LBH expression is down-regulated in the tissue and cell lines of PCa. LBH overexpression inhibits PC3M cell proliferation and tumor growth by inducing cell cycle arrest through down-regulating cyclin D1and cyclin E2 expression. LBH might be a therapeutic target and potential diagnostic marker in PCa.
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