𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Identification of Fat4 as a candidate tumor suppressor gene in breast cancers

✍ Scribed by Chao Qi; Yiwei Tony Zhu; Liping Hu; Yi-Jun Zhu


Publisher
John Wiley and Sons
Year
2009
Tongue
French
Weight
382 KB
Volume
124
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Fat, a candidate tumor suppressor in Drosophila, is a component of Hippo signaling pathway involved in controlling organ size. We found that a ∼3 Mbp deletion in mouse chromosome 3 caused tumorigenesis of a non‐tumorigenic mammary epithelial cell line. The expression of Fat4 gene, one member of the Fat family, in the deleted region was inactivated, which resulted from promoter methylation of another Fat4 allele following the deletion of one Fat4 allele. Re‐expression of Fat4 in Fat4‐deficient tumor cells suppressed the tumorigenecity whereas suppression of Fat4 expression in the non‐tumorigenic mammary epithelial cell line induced tumorigenesis. We also found that Fat4 expression was lost in a large fraction of human breast tumor cell lines and primary tumors. Loss of Fat4 expression in breast tumors was associated with human Fat4 promoter methylation. Together, these findings suggest that Fat4 is a strong candidate for a breast tumor suppressor gene. © 2008 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Epigenetic silencing of the candidate tu
✍ Beatrix Versmold; Jörg Felsberg; Thomas Mikeska; Denise Ehrentraut; Juliane Köhl 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 French ⚖ 362 KB 👁 2 views

## Abstract Extensive hypermethylation and consecutive transcriptional silencing of tumorsuppressor genes have been documented in multiple tumor entities including breast cancer. In a microarray based genome‐wide methylation analysis of five sporadic breast carcinomas we identified a hypermethylate

Identification of candidate tumor suppre
✍ Vanessa F. Bonazzi; Darryl Irwin; Nicholas K. Hayward 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 400 KB 👁 1 views

## Abstract Tumor suppressor genes (TSGs) are sometimes inactivated by transcriptional silencing through promoter hypermethylation. To identify novel methylated TSGs in melanoma, we carried out global mRNA expression profiling on a panel of 12 melanoma cell lines treated with a combination of 5‐Aza

A survey of methylated candidate tumor s
✍ Myriam Loyo; Mariana Brait; Myoung S. Kim; Kimberly L. Ostrow; Chunfa C. Jie; Al 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 French ⚖ 436 KB 👁 1 views

## Abstract Nasopharyngeal carcinoma (NPC) is a rare malignancy with unique genetic, viral and environmental characteristic that distinguishes it from other head and neck carcinomas. The clinical management of NPC remains challenging largely due to the lack of early detection strategies for this tu

Analysis of the transcription regulator,
✍ James Flanagan; Sue Healey; Joanne Young; Vicki Whitehall; Georgia Chenevix-Tren 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 French ⚖ 257 KB 👁 2 views

## Abstract Loss of heterozygosity (LOH) on the short arm of chromosome 8 occurs at high frequencies in many tumor types, including colorectal carcinoma. We have previously used microcell‐mediated chromosome transfer (MMCT) to map an approximately 7.7 Mb colorectal cancer suppressor region (CRCSR)

Characterization of C4-2 as a tumor-supp
✍ Sehgal, Anil; Keener, Cassie; Boynton, Alton L.; Young, Ronald F.; Vermeulen, Sa 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 189 KB 👁 3 views

Background: Brain tumors claimed the lives of 13,300 people in 1995. Our objective was to isolate and characterize unique tumor-suppressor genes from human brain tumors derived from patients in the United States. Methods: Differential display-polymerase chain reaction was used to isolate tumor suppr

Comparison of gene expression data from
✍ Andreas Klein; Ralf Wessel; Monika Graessmann; Martin Jürgens; Iver Petersen; Ri 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 French ⚖ 319 KB 👁 1 views

## Abstract The aim of our work was to establish a database for breast cancer gene expression data in order to compare human and mouse breast cancer. We identified human and mouse homologues genes and compared the expression profile of 24 human breast tumors with 6 WAP‐SVT/t breast tumors (WAP‐SVT/