» Articles » PMID: 25557041

Therapeutic Targeting of Tumor Suppressor Genes

Overview
Journal Cancer
Publisher Wiley
Specialty Oncology
Date 2015 Jan 6
PMID 25557041
Citations 86
Authors
Affiliations
Soon will be listed here.
Abstract

Carcinogenesis is a multistep process attributable to both gain-of-function mutations in oncogenes and loss-of-function mutations in tumor suppressor genes. Currently, most molecular targeted therapies are inhibitors of oncogenes, because inactivated tumor suppressor genes have proven harder to "drug." Nevertheless, in cancers, tumor suppressor genes undergo alteration more frequently than do oncogenes. In recent years, several promising strategies directed at tumor suppressor genes, or the pathways controlled by these genes, have emerged. Here, we describe advances in a number of different methodologies aimed at therapeutically targeting tumors driven by inactivated tumor suppressor genes.

Citing Articles

A Perspective on Therapeutic Targeting Against Ubiquitin Ligases to Stabilize Tumor Suppressor Proteins.

Ganesan I, Kiyokawa H Cancers (Basel). 2025; 17(4).

PMID: 40002221 PMC: 11853300. DOI: 10.3390/cancers17040626.


Positive Selection Shapes Breast Cancer Tumor Suppressor Genes: Unveiling Insights into BRCA1, BRCA2, and MDC1 Stability.

Fadel Y, Khaled M, Emam M, Marzouk N, Sobih S, Abd-Elaty H J Mol Evol. 2024; 93(1):100-110.

PMID: 39681652 DOI: 10.1007/s00239-024-10222-8.


Mapping in silico genetic networks of the KMT2D tumour suppressor gene to uncover novel functional associations and cancer cell vulnerabilities.

Takemon Y, Pleasance E, Gagliardi A, Hughes C, Csizmok V, Wee K Genome Med. 2024; 16(1):136.

PMID: 39578878 PMC: 11583415. DOI: 10.1186/s13073-024-01401-9.


The present and future of the Cancer Dependency Map.

Arafeh R, Shibue T, Dempster J, Hahn W, Vazquez F Nat Rev Cancer. 2024; 25(1):59-73.

PMID: 39468210 DOI: 10.1038/s41568-024-00763-x.


Biomarkers From Discovery to Clinical Application: In Silico Pre-Clinical Validation Approach in the Face of Lung Cancer.

Kori M, Gov E, Arga K, Sinha R Biomark Insights. 2024; 19:11772719241287400.

PMID: 39371614 PMC: 11452870. DOI: 10.1177/11772719241287400.


References
1.
Hollstein M, Sidransky D, Vogelstein B, Harris C . p53 mutations in human cancers. Science. 1991; 253(5015):49-53. DOI: 10.1126/science.1905840. View

2.
Morrison A, Johnson A, Johnston L, Sugino A . Pathway correcting DNA replication errors in Saccharomyces cerevisiae. EMBO J. 1993; 12(4):1467-73. PMC: 413358. DOI: 10.1002/j.1460-2075.1993.tb05790.x. View

3.
Kussie P, Gorina S, Marechal V, Elenbaas B, Moreau J, Levine A . Structure of the MDM2 oncoprotein bound to the p53 tumor suppressor transactivation domain. Science. 1996; 274(5289):948-53. DOI: 10.1126/science.274.5289.948. View

4.
Kinzler K, Vogelstein B . Cancer-susceptibility genes. Gatekeepers and caretakers. Nature. 1997; 386(6627):761, 763. DOI: 10.1038/386761a0. View

5.
Heise C, Sampson-Johannes A, Williams A, McCormick F, Von Hoff D, Kirn D . ONYX-015, an E1B gene-attenuated adenovirus, causes tumor-specific cytolysis and antitumoral efficacy that can be augmented by standard chemotherapeutic agents. Nat Med. 1997; 3(6):639-45. DOI: 10.1038/nm0697-639. View