» Articles » PMID: 23792637

Cables1 is a Tumor Suppressor Gene That Regulates Intestinal Tumor Progression in Apc(Min) Mice

Overview
Specialties Oncology
Pharmacology
Date 2013 Jun 25
PMID 23792637
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

The transformation of colonic mucosal epithelium to adenocarcinoma requires progressive oncogene activation and tumor suppressor gene inactivation. Loss of chromosome 18q is common in colon cancer but not in precancerous adenomas. A few candidate tumor suppressor genes have been identified in this region, including CABLES1 at 18q11.2-12.1. This study investigates the role of CABLES1 in an in vivo mouse model of intestinal adenocarcinoma and in human colon cancer cell culture. Apc(Min/+) mice were crossed with mice harboring targeted inactivation of the Cables1 gene (Cables1(-/-)). The intestinal tumor burden and tumor expression of β-catenin and PCNA was compared in Cables1(+/+)Apc(Min/+) and Cables1(-/-)Apc(Min/+) mice. β-catenin activity in human colon cancer cells with CABLES1 inactivation and intestinal progenitor cell function in Cables1(-/-) mice were assayed in vitro. The mean number of small intestinal tumors per mouse was 3.1 ± 0.6 in Cables1(+/+)Apc(Min/+) mice, compared with 32.4 ± 3.5 in the Cables1(-/-)Apc(Min/+) mice (P < 0.0001). Fewer colonic tumors were observed in Cables1(+/+)Apc(Min/+) mice (mean 0.6 ± 0.1) compared with the Cables1(-/-)Apc(Min/+) mice (mean 1.3 ± 0.3, P = 0.01). Tumors from Cables1(-/-)Apc(Min/+) mice demonstrated increased nuclear expression of β-catenin and an increased number of PCNA-positive cells. In vitro studies revealed that CABLES1 deficiency increased β-catenin dependent transcription and increased intestinal progenitor cell activity. Loss of Cables1 enhances tumor progression in the Apc(Min/+) mouse model and activates the Wnt/β-catenin signaling pathway. Cables1 is a tumor suppressor gene on chromosome 18q in this in vivo mouse model and likely has a similar role in human colon cancer.

Citing Articles

Clinical implications and molecular mechanism of long noncoding RNA LINC00518 and protein-coding genes in skin cutaneous melanoma by genome‑wide investigation.

Wang S, Wang Q, Zheng J, Yan L, Pan Y, Jiang D Arch Dermatol Res. 2025; 317(1):454.

PMID: 39987414 DOI: 10.1007/s00403-025-03961-1.


Molecular Complexity of Colorectal Cancer: Pathways, Biomarkers, and Therapeutic Strategies.

Yang Z, Wang X, Zhou H, Jiang M, Wang J, Sui B Cancer Manag Res. 2024; 16:1389-1403.

PMID: 39403607 PMC: 11472760. DOI: 10.2147/CMAR.S481656.


Insights into Gene Regulation under Temozolomide-Promoted Cellular Dormancy and Its Connection to Stemness in Human Glioblastoma.

Kubelt C, Hellmold D, Esser D, Ahmeti H, Synowitz M, Held-Feindt J Cells. 2023; 12(11).

PMID: 37296610 PMC: 10252797. DOI: 10.3390/cells12111491.


Tumor-Suppressive Functions of the Aryl Hydrocarbon Receptor (AhR) and AhR as a Therapeutic Target in Cancer.

Elson D, Kolluri S Biology (Basel). 2023; 12(4).

PMID: 37106727 PMC: 10135996. DOI: 10.3390/biology12040526.


11-Cl-BBQ, a select modulator of AhR-regulated transcription, suppresses lung cancer cell growth via activation of p53 and p27.

Nguyen B, Stevens B, Elson D, Finlay D, Gamble J, Kopparapu P FEBS J. 2022; 290(8):2064-2084.

PMID: 36401795 PMC: 10807707. DOI: 10.1111/febs.16683.


References
1.
Sato T, Vries R, Snippert H, van de Wetering M, Barker N, Stange D . Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche. Nature. 2009; 459(7244):262-5. DOI: 10.1038/nature07935. View

2.
Takaku K, Oshima M, Miyoshi H, Matsui M, Seldin M, Taketo M . Intestinal tumorigenesis in compound mutant mice of both Dpc4 (Smad4) and Apc genes. Cell. 1998; 92(5):645-56. DOI: 10.1016/s0092-8674(00)81132-0. View

3.
Tan D, Kirley S, Li Q, Ramnath N, Slocum H, Brooks J . Loss of cables protein expression in human non-small cell lung cancer: a tissue microarray study. Hum Pathol. 2003; 34(2):143-9. DOI: 10.1053/hupa.2003.26. View

4.
Sato T, van Es J, Snippert H, Stange D, Vries R, van den Born M . Paneth cells constitute the niche for Lgr5 stem cells in intestinal crypts. Nature. 2010; 469(7330):415-8. PMC: 3547360. DOI: 10.1038/nature09637. View

5.
Zukerberg L, DeBernardo R, Kirley S, DApuzzo M, Lynch M, Littell R . Loss of cables, a cyclin-dependent kinase regulatory protein, is associated with the development of endometrial hyperplasia and endometrial cancer. Cancer Res. 2004; 64(1):202-8. DOI: 10.1158/0008-5472.can-03-2833. View