𝔖 Bobbio Scriptorium
✦   LIBER   ✦

GADD45A is a mediator of CD437 induced apoptosis in ovarian carcinoma cells

✍ Scribed by Tianying Jiang; Dianne Robert Soprano; Kenneth J. Soprano


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
417 KB
Volume
212
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Ovarian cancer is one of the leading causes of cancer death in women. A number of studies have suggested that synthetic retinoids may play an important role as an ovarian cancer chemotherapeutic agent. The synthetic retinoid CD 437 induces apoptosis in ovarian tumor cells by a mechanism that is not completely understood. In this study we demonstrate that CD437 treatment leads to an increase in GADD45A and GADD45B mRNA expression in CA‐OV3 cells but not in CA‐CD437R cells, a cell line which is resistant to CD437. This induction is specific to CD437 since no change in expression of either GADD45A or GADD45B was observed with either all__‐trans__‐RA or 4‐HPR treatment. Western blot analysis demonstrated that the induction of GADD45A mRNA in the CA‐OV3 cell line by CD437 was accompanied by an increase in GADD45A protein. Upregulation of GADD45A by CD437 is regulated at least in part at the post‐transcriptional level. In contrast, CD437 regulates GADD45B expression by different mechanisms. The importance of GADD45A induction in mediating apoptosis was demonstrated in CA‐OV3 cells overexpressing GADD45A antisense RNA (GADD45A‐AS cells). Our results suggest that induction of GADD45A expression might play a role in mediating the apoptotic response of ovarian cancer cells to the synthetic retinoid CD437. J. Cell. Physiol. 212:771–779, 2007. © 2007 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Induction of apoptosis in ovarian carcin
✍ William F. Holmes; Marcia I. Dawson; Dianne Robert Soprano; Kenneth J. Soprano 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 175 KB 👁 2 views

Retinoids have great promise in the area of cancer therapy and chemoprevention. These natural and synthetic derivatives of vitamin A have been shown to play an important role in regulating cell differentiation and proliferation. While all-trans-retinoic acid (ATRA) has been demonstrated to inhibit t

Adenoviral-mediated gene transfer of Gad
✍ Yunfeng Li; Haili Qian; Xiao Li; Haijuan Wang; Jing Yu; Yongjun Liu; Xueyan Zhan 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 433 KB 👁 1 views

## Abstract ## Background The extremely poor prognosis of patients with pancreatic ductal adenocarcinoma indicates the need for novel therapeutic approaches. The growth arrest and DNA damage‐inducible (Gadd) gene __Gadd45a__ is a member of a group of genes that are induced by DNA damaging agents a

Mechanism of taxol-induced apoptosis in
✍ Hak Jun Ahn; Yeong Shik Kim; Joung-Uk Kim; Sung Min Han; Jin Woo Shin; Hyun Ok Y 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 319 KB

## Abstract Taxol is extensively used clinically for chemotherapy of patients with ovarian, breast, and lung cancer. Although taxol induces apoptosis of cancer cells, its exact mechanism of action is not yet known. To determine the mechanism of action of taxol in ovarian cancer, we tested the effec

Retinoic acid induced repression of AP-1
✍ Carmilia Jiménez Ramírez; Juliet M. Haberbusch; Dianne Robert Soprano; Kenneth J 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 278 KB

## Abstract In previous studies we have shown that __all__‐__trans__ retinoic acid (__at__RA)‐treatment of the __at__RA‐sensitive ovarian carcinoma cell line CA‐OV3 repressed AP‐1 activity by about 50%, while a similar effect was not observed in the __at__RA‐resistant ovarian carcinoma cell line, S

Comparison of the mechanism of induction
✍ William F. Holmes; Dianne Robert Soprano; Kenneth J. Soprano 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 477 KB

## Abstract All‐trans‐retinoic acid (ATRA) has been shown to inhibit the growth of a number of ovarian tumor cell lines while others have been found to be resistant to retinoid suppression of growth. Interestingly, two synthetic retinoids, CD437 and 4‐HPR, inhibit the growth of both ATRA‐sensitive