» Articles » PMID: 30759745

Semaphorin 3C As a Therapeutic Target in Prostate and Other Cancers

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2019 Feb 15
PMID 30759745
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The semaphorins represent a large family of signaling molecules with crucial roles in neuronal and cardiac development. While normal semaphorin function pertains largely to development, their involvement in malignancy is becoming increasingly evident. One member, Semaphorin 3C (SEMA3C), has been shown to drive a number of oncogenic programs, correlate inversely with cancer prognosis, and promote the progression of multiple different cancer types. This report surveys the body of knowledge surrounding SEMA3C as a therapeutic target in cancer. In particular, we summarize SEMA3C's role as an autocrine andromedin in prostate cancer growth and survival and provide an overview of other cancer types that SEMA3C has been implicated in including pancreas, brain, breast, and stomach. We also propose molecular strategies that could potentially be deployed against SEMA3C as anticancer agents such as biologics, small molecules, monoclonal antibodies and antisense oligonucleotides. Finally, we discuss important considerations for the inhibition of SEMA3C as a cancer therapeutic agent.

Citing Articles

Downregulation of semaphorin 4A in keratinocytes reflects the features of non-lesional psoriasis.

Kume M, Koguchi-Yoshioka H, Nakai S, Matsumura Y, Tanemura A, Yokoi K Elife. 2024; 13.

PMID: 39737847 PMC: 11687936. DOI: 10.7554/eLife.97654.


Construction and validation of a prognostic signature based on microvascular invasion and immune-related genes in hepatocellular carcinoma.

Li H, Qiao L, Kong M, Fang H, Yan Z, Guo R Sci Rep. 2024; 14(1):26994.

PMID: 39506070 PMC: 11541849. DOI: 10.1038/s41598-024-78467-3.


A Pilot Study of the Role of Semaphorin 4A (sema4A) and 3C (sema3C) in Non-Muscle-Invasive Bladder Cancer (NMIBC).

Purpurowicz P, Kaminski T, Kordan W, Korzekwa A, Purpurowicz Z, Jablonowski Z Biomedicines. 2024; 12(10).

PMID: 39457718 PMC: 11504222. DOI: 10.3390/biomedicines12102407.


Semaphorins and Their Roles in Breast Cancer: Implications for Therapy Resistance.

Aiyappa-Maudsley R, McLoughlin L, Hughes T Int J Mol Sci. 2023; 24(17).

PMID: 37685898 PMC: 10487980. DOI: 10.3390/ijms241713093.


Perineural invasion in colorectal cancer: mechanisms of action and clinical relevance.

Wang H, Huo R, He K, Cheng L, Zhang S, Yu M Cell Oncol (Dordr). 2023; 47(1):1-17.

PMID: 37610689 PMC: 10899381. DOI: 10.1007/s13402-023-00857-y.


References
1.
Li K, Chen M, Li L, Lu M, Shao C, Su Z . The predictive value of semaphorins 3 expression in biopsies for biochemical recurrence of patients with low- and intermediate-risk prostate cancer. Neoplasma. 2013; 60(6):683-9. DOI: 10.4149/neo_2013_087. View

2.
Bao S, Wu Q, McLendon R, Hao Y, Shi Q, Hjelmeland A . Glioma stem cells promote radioresistance by preferential activation of the DNA damage response. Nature. 2006; 444(7120):756-60. DOI: 10.1038/nature05236. View

3.
Esselens C, Malapeira J, Colome N, Casal C, Rodriguez-Manzaneque J, Canals F . The cleavage of semaphorin 3C induced by ADAMTS1 promotes cell migration. J Biol Chem. 2009; 285(4):2463-73. PMC: 2807303. DOI: 10.1074/jbc.M109.055129. View

4.
Toyofuku T, Yoshida J, Sugimoto T, Yamamoto M, Makino N, Takamatsu H . Repulsive and attractive semaphorins cooperate to direct the navigation of cardiac neural crest cells. Dev Biol. 2008; 321(1):251-62. DOI: 10.1016/j.ydbio.2008.06.028. View

5.
Wang Y, He H, Srivastava N, Vikarunnessa S, Chen Y, Jiang J . Plexins are GTPase-activating proteins for Rap and are activated by induced dimerization. Sci Signal. 2012; 5(207):ra6. PMC: 3413289. DOI: 10.1126/scisignal.2002636. View