Literature DB >> 19143644

PI3K inhibitors for cancer treatment: where do we stand?

Sauveur-Michel Maira1, Frédéric Stauffer, Christian Schnell, Carlos García-Echeverría.   

Abstract

In contrast with cytotoxic agents that do not differentiate between normal proliferating and tumour cells, targeted therapies primarily exert their actions in cancer cells. Initiation and maintenance of tumours are due to genetic alterations in specific loci. The identification of the genes in which these alterations occur has opened new opportunities for cancer treatment. The PI3K (phosphoinositide 3-kinase) pathway is often overactive in human cancers, and various genetic alterations have been found to cause this. In all cases, PI3K inhibition is considered to be one of the most promising targeted therapies for cancer treatment. The present mini-review provides an update on new PI3K inhibitors currently in or entering clinical development. Recent discoveries, challenges and future prospects will be discussed.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19143644     DOI: 10.1042/BST0370265

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  46 in total

1.  A chemical biology approach identified PI3K as a potential therapeutic target for neurofibromatosis type 2.

Authors:  Alejandra M Petrilli; Marisa A Fuse; Mathew S Donnan; Marga Bott; Nicklaus A Sparrow; Daniel Tondera; Julia Huffziger; Corina Frenzel; C Siobhan Malany; Christophe J Echeverri; Layton Smith; Cristina Fernández-Valle
Journal:  Am J Transl Res       Date:  2014-10-11       Impact factor: 4.060

Review 2.  Preclinical studies identify novel targeted pharmacological strategies for treatment of human malignant pleural mesothelioma.

Authors:  Roberto E Favoni; Antonio Daga; Paolo Malatesta; Tullio Florio
Journal:  Br J Pharmacol       Date:  2012-05       Impact factor: 8.739

Review 3.  Translational control in cancer.

Authors:  Deborah Silvera; Silvia C Formenti; Robert J Schneider
Journal:  Nat Rev Cancer       Date:  2010-04       Impact factor: 60.716

4.  Inhibition of class IA PI3K enzymes in non-small cell lung cancer cells uncovers functional compensation among isoforms.

Authors:  Christopher Stamatkin; Kelley L Ratermann; Colleen W Overley; Esther P Black
Journal:  Cancer Biol Ther       Date:  2015-07-15       Impact factor: 4.742

5.  Downregulation of DEC1 contributes to the neurotoxicity induced by MPP+ by suppressing PI3K/Akt/GSK3β pathway.

Authors:  Zhu Zhu; Yu-Wen Wang; Ding-Hao Ge; Ming Lu; Wei Liu; Jing Xiong; Gang Hu; Xiao-Ping Li; Jian Yang
Journal:  CNS Neurosci Ther       Date:  2017-07-21       Impact factor: 5.243

6.  Effect of kinase inhibitors on the therapeutic properties of monoclonal antibodies.

Authors:  Minh Ngoc Duong; Eva-Laure Matera; Doriane Mathé; Anne Evesque; Sandrine Valsesia-Wittmann; Béatrice Clémenceau; Charles Dumontet
Journal:  MAbs       Date:  2015       Impact factor: 5.857

Review 7.  mTOR: dissecting regulation and mechanism of action to understand human disease.

Authors:  Deborah C I Goberdhan; C A Richard Boyd
Journal:  Biochem Soc Trans       Date:  2009-02       Impact factor: 5.407

Review 8.  Brain tumor stem cells as therapeutic targets in models of glioma.

Authors:  Dan Richard Laks; Koppany Visnyei; Harley Ian Kornblum
Journal:  Yonsei Med J       Date:  2010-09       Impact factor: 2.759

Review 9.  Caspase control: protagonists of cancer cell apoptosis.

Authors:  M V Fiandalo; N Kyprianou
Journal:  Exp Oncol       Date:  2012-10

10.  Rapamycin by itself and additively in combination with carboplatin inhibits the growth of ovarian cancer cells.

Authors:  Peter W Schlosshauer; Wei Li; Kai-Ti Lin; Joseph L-K Chan; Lu-Hai Wang
Journal:  Gynecol Oncol       Date:  2009-07-02       Impact factor: 5.482

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.