Literature DB >> 10638484

RAS inhibitors in hematologic cancers: biologic considerations and clinical applications.

D M Beaupre1, R Kurzrock.   

Abstract

As the molecular mechanisms responsible for the development and propagation of cancer are becoming elucidated, the nascent field of gene-directed therapy is emerging. Recently, several investigators have described inhibitors of the Ras protein. This molecule has been targeted because RAS is one of the most commonly mutated oncogenes in human neoplasia. In this review, we will discuss the role of Ras in the pathogenesis of hematologic neoplasms, and the biology behind the development of novel compounds which specifically suppress Ras function.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10638484     DOI: 10.1023/a:1006319116226

Source DB:  PubMed          Journal:  Invest New Drugs        ISSN: 0167-6997            Impact factor:   3.850


  78 in total

Review 1.  Inhibitors of prenyl transferases.

Authors:  S Sebti; A D Hamilton
Journal:  Curr Opin Oncol       Date:  1997-11       Impact factor: 3.645

2.  Expression of normal and mutant ras proteins in human acute leukemia.

Authors:  W P Shen; T H Aldrich; G Venta-Perez; B R Franza; M E Furth
Journal:  Oncogene       Date:  1987-05       Impact factor: 9.867

3.  Suppression of chronic myelogenous leukemia colony growth by interleukin-1 (IL-1) receptor antagonist and soluble IL-1 receptors: a novel application for inhibitors of IL-1 activity.

Authors:  Z Estrov; R Kurzrock; M Wetzler; H Kantarjian; M Blake; D Harris; J U Gutterman; M Talpaz
Journal:  Blood       Date:  1991-09-15       Impact factor: 22.113

4.  [Gene diagnosis of pancreatic adenocarcinoma].

Authors:  Z Y Wang; T H Liu; Q C Cui
Journal:  Zhonghua Bing Li Xue Za Zhi       Date:  1994-10

Review 5.  Role of interleukin-1 inhibitory molecules in therapy of acute and chronic myelogenous leukemia.

Authors:  Z Estrov; R Kurzrock; M Talpaz
Journal:  Leuk Lymphoma       Date:  1993-08

6.  The Ras antagonist S-farnesylthiosalicylic acid induces inhibition of MAPK activation.

Authors:  M Gana-Weisz; R Haklai; D Marciano; Y Egozi; G Ben-Baruch; Y Kloog
Journal:  Biochem Biophys Res Commun       Date:  1997-10-29       Impact factor: 3.575

7.  Genetic analysis is consistent with the hypothesis that NF1 limits myeloid cell growth through p21ras.

Authors:  R Kalra; D C Paderanga; K Olson; K M Shannon
Journal:  Blood       Date:  1994-11-15       Impact factor: 22.113

8.  Differential effects of monoterpenes and lovastatin on RAS processing.

Authors:  R J Hohl; K Lewis
Journal:  J Biol Chem       Date:  1995-07-21       Impact factor: 5.157

9.  Development of highly potent inhibitors of Ras farnesyltransferase possessing cellular and in vivo activity.

Authors:  K Leftheris; T Kline; G D Vite; Y H Cho; R S Bhide; D V Patel; M M Patel; R J Schmidt; H N Weller; M L Andahazy; J M Carboni; J L Gullo-Brown; F Y Lee; C Ricca; W C Rose; N Yan; M Barbacid; J T Hunt; C A Meyers; B R Seizinger; R Zahler; V Manne
Journal:  J Med Chem       Date:  1996-01-05       Impact factor: 7.446

10.  SSCP detection of N-ras promoter mutations in AML patients.

Authors:  J Thorn; P Molloy; H Iland
Journal:  Exp Hematol       Date:  1995-09       Impact factor: 3.084

View more
  1 in total

1.  Pharmacological or genetic inhibition of hypoxia signaling attenuates oncogenic RAS-induced cancer phenotypes.

Authors:  Jun-Yi Zhu; Xiaohu Huang; Yulong Fu; Yin Wang; Pan Zheng; Yang Liu; Zhe Han
Journal:  Dis Model Mech       Date:  2021-11-19       Impact factor: 5.758

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.