Literature DB >> 18798058

RAS: target for cancer therapy.

Nandita Saxena1, Sitanshu Sekhar Lahiri, Shashank Hambarde, Rajendra Prasad Tripathi.   

Abstract

The RAS protein controls signaling pathway are major player in cell growth, its regulation and malignant transformation. Any activation in RAS brings alteration in upstream or downstream signaling component. Activating mutation in RAS is found in approximately 30% of human cancer. RAS plays essential role in tumor maintenance and is therefore an appropriate target for anticancer therapy. Among the anti-RAS strategies that are under evaluation in the clinic are pharmacologic inhibitors designed to prevent: (1) association with the plasma membrane (prenylation and post prenylation inhibitors). (2) Downstream signaling (kinase inhibitor), (3) upstream pathway (kinase inhibitor and monoclonal antibody), (4) Expression of RAS or other component of pathway (siRNA and antisense oligonucleotide). Several of these new therapeutic agents are showing promising result in the clinic and many more are on the way. Here, we review the current status and new hopes for targeting RAS as an anticancer drug.

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Year:  2008        PMID: 18798058     DOI: 10.1080/07357900802087275

Source DB:  PubMed          Journal:  Cancer Invest        ISSN: 0735-7907            Impact factor:   2.176


  35 in total

1.  Ubiquitination: Added complexity in Ras and Rho family GTPase function.

Authors:  Michelle de la Vega; James F Burrows; James A Johnston
Journal:  Small GTPases       Date:  2011-07-01

Review 2.  Synthetic lethal interactions for the development of cancer therapeutics: biological and methodological advancements.

Authors:  Shinji Mizuarai; Hidehito Kotani
Journal:  Hum Genet       Date:  2010-10-26       Impact factor: 4.132

3.  LEOPARD Syndrome: Clinical Features and Gene Mutations.

Authors:  E Martínez-Quintana; F Rodríguez-González
Journal:  Mol Syndromol       Date:  2012-08-29

4.  Analysis of binding site hot spots on the surface of Ras GTPase.

Authors:  Greg Buhrman; Casey O'Connor; Brandon Zerbe; Bradley M Kearney; Raeanne Napoleon; Elizaveta A Kovrigina; Sandor Vajda; Dima Kozakov; Evgenii L Kovrigin; Carla Mattos
Journal:  J Mol Biol       Date:  2011-09-16       Impact factor: 5.469

5.  PI3K regulation of RAC1 is required for KRAS-induced pancreatic tumorigenesis in mice.

Authors:  Chia-Yen C Wu; Eileen S Carpenter; Kenneth K Takeuchi; Christopher J Halbrook; Louise V Peverley; Harold Bien; Jason C Hall; Kathleen E DelGiorno; Debjani Pal; Yan Song; Chanjuan Shi; Richard Z Lin; Howard C Crawford
Journal:  Gastroenterology       Date:  2014-08-27       Impact factor: 22.682

Review 6.  Genetic alterations in the phosphatidylinositol-3 kinase/Akt pathway in thyroid cancer.

Authors:  Mingzhao Xing
Journal:  Thyroid       Date:  2010-07       Impact factor: 6.568

7.  Argonaute2 is a potential target for siRNA-based cancer therapy for HT1080 human fibrosarcoma.

Authors:  Tatsuaki Tagami; Takuya Suzuki; Kiyomi Hirose; Jose Mario Barichello; Naoshi Yamazaki; Tomohiro Asai; Naoto Oku; Tatsuhiro Ishida; Hiroshi Kiwada
Journal:  Drug Deliv Transl Res       Date:  2011-08       Impact factor: 4.617

8.  The role of neurofibromin in N-Ras mediated AP-1 regulation in malignant peripheral nerve sheath tumors.

Authors:  Janice M Kraniak; Daochun Sun; Raymond R Mattingly; John J Reiners; Michael A Tainsky
Journal:  Mol Cell Biochem       Date:  2010-08-01       Impact factor: 3.396

Review 9.  Lessons from mouse models of thyroid cancer.

Authors:  Caroline S Kim; Xuguang Zhu
Journal:  Thyroid       Date:  2009-12       Impact factor: 6.568

Review 10.  Modeling thyroid cancer in the mouse.

Authors:  X-G Zhu; S-Y Cheng
Journal:  Horm Metab Res       Date:  2009-04-08       Impact factor: 2.936

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