Literature DB >> 22494490

An overview of the mTOR pathway as a target in cancer therapy.

Ryan D Gentzler1, Jessica K Altman, Leonidas C Platanias.   

Abstract

INTRODUCTION: The mammalian target of rapamycin (mTOR) signaling cascade is a key regulatory pathway controlling initiation of mRNA translation in mammalian cells. The mTOR inhibitor rapamycin and its derivatives have shown potent antineoplastic activities in many preclinical models and clinical trials. First-generation mTOR inhibitors are now FDA-approved for the treatment of renal cell carcinoma. AREAS COVERED: This article reviews the components of the mTOR pathway and their normal functions, highlighting the most common alterations in the pathway, seen in various human malignancies. It also discusses elements and effectors of this signaling cascade and reviews the therapeutic relevance of pharmacological inhibitors of the pathway in several malignancies, including lymphomas, leukemias, sarcomas, renal cell carcinoma, and breast cancer. EXPERT OPINION: mTOR targeting is a highly promising therapeutic approach. First-generation mTOR inhibitors have already shown substantial activity in the treatment of certain tumors, while the emergence of second-generation catalytic mTOR inhibitors provides a better approach to target the pathway in malignant cells and has raised the potential for better clinical outcomes in the future.

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Year:  2012        PMID: 22494490     DOI: 10.1517/14728222.2012.677439

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  16 in total

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Review 2.  PI3K and cancer: lessons, challenges and opportunities.

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Review 3.  Intersection of mTOR and STAT signaling in immunity.

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Review 4.  Targeting mTOR signaling pathways and related negative feedback loops for the treatment of acute myeloid leukemia.

Authors:  Benedito A Carneiro; Jason B Kaplan; Jessica K Altman; Francis J Giles; Leonidas C Platanias
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Review 5.  Tuberous Sclerosis: A New Frontier in Targeted Treatment of Autism.

Authors:  Peter E Davis; Jurriaan M Peters; Darcy A Krueger; Mustafa Sahin
Journal:  Neurotherapeutics       Date:  2015-07       Impact factor: 7.620

6.  Therapeutic silencing of mTOR by systemically administered siRNA-loaded neutral liposomal nanoparticles inhibits DMBA-induced mammary carcinogenesis.

Authors:  Roja Sahu; Shakti Prasad Pattanayak; Shivesh Jha
Journal:  Br J Cancer       Date:  2022-10-19       Impact factor: 9.075

7.  Too much or too little: harnessing senescence to control oncogene-driven cancer.

Authors:  Katherine M Hannan; Richard B Pearson
Journal:  Cell Cycle       Date:  2012-08-16       Impact factor: 4.534

Review 8.  mTOR Signaling in Protein Translation Regulation: Implications in Cancer Genesis and Therapeutic Interventions.

Authors:  Mehvish Showkat; Mushtaq A Beigh; Khurshid I Andrabi
Journal:  Mol Biol Int       Date:  2014-11-20

9.  PI3K/mTOR pathway inhibitors sensitize chronic myeloid leukemia stem cells to nilotinib and restore the response of progenitors to nilotinib in the presence of stem cell factor.

Authors:  K Airiau; F-X Mahon; M Josselin; M Jeanneteau; F Belloc
Journal:  Cell Death Dis       Date:  2013-10-03       Impact factor: 8.469

10.  Phospho-mTOR in non-tumour and tumour bladder urothelium: Pattern of expression and impact on urothelial bladder cancer patients.

Authors:  Julieta Afonso; Adhemar Longatto-Filho; Vitor Moreira DA Silva; Teresina Amaro; Lúcio L Santos
Journal:  Oncol Lett       Date:  2014-07-30       Impact factor: 2.967

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