Literature DB >> 30074275

Disrupting cholesterol esterification by bitter melon suppresses triple-negative breast cancer cell growth.

So Hee Shim1, Subhayan Sur1, Robert Steele1, Carolyn J Albert2, Chunfa Huang3, David A Ford2, Ratna B Ray1,3.   

Abstract

Triple negative breast cancer (TNBC) is aggressive with a worse prognosis. We have recently shown that bitter melon extract (BME) treatment was more effective in inhibition of TNBC tumor growth in mouse models as compared to ER positive breast tumor growth. Aberrant dysregulation of lipid metabolism is associated with breast cancer progression, however, anti-cancer mechanism of BME linking lipid metabolism in breast cancer growth remains unexplored. Here, we observed that accumulation of esterified cholesterol was reduced in BME treated TNBC cell lines as compared to control cells. We next evaluated expression levels of acyl-CoA: cholesterol acyltransferase 1 (ACAT-1) in TNBC cells treated with BME. Our results demonstrated that BME treatment inhibited ACAT-1 expression in TNBC cells. Subsequently, we found that sterol regulatory element-binding proteins-1 and -2, and FASN was significantly reduced in BME treated TNBC cell lines. Low-density lipoprotein receptor was also downregulated in BME treated TNBC cells as compared to control cells. We further demonstrated that BME feeding reduced tumor growth in TNBC mammospheres implanted into NSG mice, and inhibits ACAT-1 expression. To our knowledge, this is the first report demonstrating BME suppresses TNBC cell growth through ACAT-1 inhibition, and have potential for additional therapeutic regimen against human breast cancer.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  Acyl-CoA: cholesterol acyltransferase 1; cholesteryl ester; sterol regulatory element-binding proteins; triple-negative breast cancer

Mesh:

Substances:

Year:  2018        PMID: 30074275     DOI: 10.1002/mc.22882

Source DB:  PubMed          Journal:  Mol Carcinog        ISSN: 0899-1987            Impact factor:   4.784


  9 in total

1.  Cholesterol homeostasis and cancer: a new perspective on the low-density lipoprotein receptor.

Authors:  Jia Gu; Neng Zhu; Hong-Fang Li; Tan-Jun Zhao; Chan-Juan Zhang; Duan-Fang Liao; Li Qin
Journal:  Cell Oncol (Dordr)       Date:  2022-07-22       Impact factor: 7.051

2.  Interaction Proteomics Identifies ERbeta Association with Chromatin Repressive Complexes to Inhibit Cholesterol Biosynthesis and Exert An Oncosuppressive Role in Triple-negative Breast Cancer.

Authors:  Elena Alexandrova; Giorgio Giurato; Pasquale Saggese; Giovanni Pecoraro; Jessica Lamberti; Maria Ravo; Francesca Rizzo; Domenico Rocco; Roberta Tarallo; Tuula A Nyman; Francesca Collina; Monica Cantile; Maurizio Di Bonito; Gerardo Botti; Giovanni Nassa; Alessandro Weisz
Journal:  Mol Cell Proteomics       Date:  2019-12-02       Impact factor: 5.911

Review 3.  Cholesterol Metabolic Reprogramming in Cancer and Its Pharmacological Modulation as Therapeutic Strategy.

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5.  Inhibition of the key metabolic pathways, glycolysis and lipogenesis, of oral cancer by bitter melon extract.

Authors:  Subhayan Sur; Hiroshi Nakanishi; Colin Flaveny; Joseph E Ippolito; Jane McHowat; David A Ford; Ratna B Ray
Journal:  Cell Commun Signal       Date:  2019-10-21       Impact factor: 5.712

Review 6.  Bitter Melon (Momordica Charantia), a Nutraceutical Approach for Cancer Prevention and Therapy.

Authors:  Subhayan Sur; Ratna B Ray
Journal:  Cancers (Basel)       Date:  2020-07-27       Impact factor: 6.639

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Authors:  Gaia Iazzolino; Unai Mendibil; Blanca Arnaiz; Ane Ruiz-de-Angulo; Mikel Azkargorta; Kepa B Uribe; Neda Khatami; Felix Elortza; Beatriz Olalde; Vanessa Gomez-Vallejo; Jordi Llop; Ander Abarrategi
Journal:  Front Oncol       Date:  2022-08-18       Impact factor: 5.738

Review 8.  Cholesterol Metabolism as a Potential Therapeutic Target and a Prognostic Biomarker for Cancer Immunotherapy.

Authors:  Huixian Zhang; Wencheng Zhao; Xingya Li; Yayi He
Journal:  Onco Targets Ther       Date:  2021-06-21       Impact factor: 4.147

9.  MMP-7 derived peptides with MHC class-I binding motifs from canine mammary tumor tissue elicit strong antigen-specific T-cell responses in BALB/c mice.

Authors:  Pavan Kumar Yadav; Shishir Kumar Gupta; Saroj Kumar; Mayukh Ghosh; Brijesh Singh Yadav; Dinesh Kumar; Ajay Kumar; Mohini Saini; Meena Kataria
Journal:  Mol Cell Biochem       Date:  2020-09-24       Impact factor: 3.396

  9 in total

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