Literature DB >> 27194555

Review of PI3K/mTOR Inhibitors Entering Clinical Trials to Treat Triple Negative Breast Cancers.

Amélie Fouqué, Mickael Jean, Pierre van de Weghe, Patrick Legembre1.   

Abstract

BACKGROUND: Constitutive activation of the PI3K/mTOR signaling pathway is observed in most, if not all, breast cancers. Accordingly, many PI3K and/or mTOR inhibitors have entered clinical trials, and completed studies should soon reveal the efficacy of these new drug families in the treatment of cancer patients.
OBJECTIVE: We present the PI3K/Akt/mTOR signaling pathway and the structure and the anti-tumor efficiency of some mTOR inhibitors such as rapalogues and competitive inhibitors, which have entered clinical trials. We also discuss some of the clinical trial results associated with these molecules mainly focusing on studies performed on relapsing breast cancer patients - but not only.
RESULTS: Most of the clinical trials with PI3K/mTOR inhibitors alone or in combination with chemotherapies were performed in heavily pre-treated patients and revealed non-negligible amounts of partial responses and long-term stable disease for these patients. Therefore, these compounds seem to prevent tumor growth and survival of cancer cells in Human, representing a new range of anti-tumor drugs that can be utilized not only as first-line treatments but as second- and third-line agents for patients who relapse.
CONCLUSION: Drugs inhibiting the PI3K/mTOR signaling pathway may represent tailored anti-tumor agents, paving the way for their clinical application in different tumor types.

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Year:  2016        PMID: 27194555     DOI: 10.2174/1574892811666160519113731

Source DB:  PubMed          Journal:  Recent Pat Anticancer Drug Discov        ISSN: 1574-8928            Impact factor:   4.169


  9 in total

1.  Dual inhibition of ERK1/2 and AKT pathways is required to suppress the growth and survival of endometriotic cells and lesions.

Authors:  Joe A Arosh; Sakhila K Banu
Journal:  Mol Cell Endocrinol       Date:  2018-12-20       Impact factor: 4.102

2.  Loss of PTEN in high grade advanced stage triple negative breast ductal cancers in African American women.

Authors:  Farhan Khan; Ashwini Esnakula; Luisel J Ricks-Santi; Rabia Zafar; Yasmine Kanaan; Tammey Naab
Journal:  Pathol Res Pract       Date:  2018-03-27       Impact factor: 3.250

3.  Rapalogs Potential as Practical Alternatives to Rapamycin.

Authors:  Ahmed F Abdel-Magid
Journal:  ACS Med Chem Lett       Date:  2019-05-24       Impact factor: 4.345

4.  Molecular determinants of drug response in TNBC cell lines.

Authors:  Nathan M Merrill; Eric J Lachacz; Nathalie M Vandecan; Peter J Ulintz; Liwei Bao; John P Lloyd; Joel A Yates; Aki Morikawa; Sofia D Merajver; Matthew B Soellner
Journal:  Breast Cancer Res Treat       Date:  2019-10-26       Impact factor: 4.872

5.  YAP1 inhibition radiosensitizes triple negative breast cancer cells by targeting the DNA damage response and cell survival pathways.

Authors:  Daniel Andrade; Meghna Mehta; James Griffith; Janani Panneerselvam; Akhil Srivastava; Tae-Dong Kim; Ralf Janknecht; Terence Herman; Rajagopal Ramesh; Anupama Munshi
Journal:  Oncotarget       Date:  2017-10-20

Review 6.  Triple negative breast cancer: shedding light onto the role of pi3k/akt/mtor pathway.

Authors:  Daniela Massihnia; Antonio Galvano; Daniele Fanale; Alessandro Perez; Marta Castiglia; Lorena Incorvaia; Angela Listì; Sergio Rizzo; Giuseppe Cicero; Viviana Bazan; Sergio Castorina; Antonio Russo
Journal:  Oncotarget       Date:  2016-09-13

Review 7.  NAD/NAMPT and mTOR Pathways in Melanoma: Drivers of Drug Resistance and Prospective Therapeutic Targets.

Authors:  Alice Indini; Irene Fiorilla; Luca Ponzone; Enzo Calautti; Valentina Audrito
Journal:  Int J Mol Sci       Date:  2022-09-01       Impact factor: 6.208

Review 8.  The "Yin and Yang" of Natural Compounds in Anticancer Therapy of Triple-Negative Breast Cancers.

Authors:  Elizabeth Varghese; Samson Mathews Samuel; Mariam Abotaleb; Sohaila Cheema; Ravinder Mamtani; Dietrich Büsselberg
Journal:  Cancers (Basel)       Date:  2018-09-21       Impact factor: 6.639

9.  Increased SNAT1 is a marker of human osteosarcoma and potential therapeutic target.

Authors:  Miaomiao Wang; Ying Liu; Wenzheng Fang; Ke Liu; Xiaodong Jiao; Zhan Wang; Jiejun Wang; Yuan-Sheng Zang
Journal:  Oncotarget       Date:  2017-09-05
  9 in total

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