Literature DB >> 18991783

Targeting heparan sulfate proteoglycans in breast cancer treatment.

Chuay-Yeng Koo1, Yin-Ping Sen, Boon-Huat Bay, George W Yip.   

Abstract

Breast carcinoma is one of the leading causes of mortality among female cancers globally. Heparan sulfate proteoglycans, found predominantly on cell surfaces and in the extracellular matrix, are known to regulate breast cancer cellular behavior. Many studies have shown that these molecules serve as potential biomarkers for breast cancer. In addition, they have aberrant expression patterns and participate in various molecular signaling pathways in tumor progression. There is substantial interest in targeting heparan sulfate proteoglycans for cancer treatment, which needs to be tailored according to the roles that each proteoglycan plays in cancer biology. Current clinical trials using phosphomannopentaose sulfate, a heparan sulfate mimic, and various forms of heparin have produced promising results in breast cancer patients. Besides heparan sulfate chains, novel therapeutic agents could potentially be developed to regulate the proteoglycan core proteins as well as enzymes that modify heparan sulfation patterns. This review discusses the current use and future prospective applications of heparan sulfate proteoglycans, which have been recently patented, as therapeutic targets in breast cancer treatment.

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Year:  2008        PMID: 18991783     DOI: 10.2174/157489208786242278

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


  12 in total

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2.  A computational framework for heparan sulfate sequencing using high-resolution tandem mass spectra.

Authors:  Han Hu; Yu Huang; Yang Mao; Xiang Yu; Yongmei Xu; Jian Liu; Chengli Zong; Geert-Jan Boons; Cheng Lin; Yu Xia; Joseph Zaia
Journal:  Mol Cell Proteomics       Date:  2014-06-12       Impact factor: 5.911

3.  Mastoparan is a membranolytic anti-cancer peptide that works synergistically with gemcitabine in a mouse model of mammary carcinoma.

Authors:  Ashley L Hilchie; Andrew J Sharon; Evan F Haney; David W Hoskin; Marcel B Bally; Octavio L Franco; Jennifer A Corcoran; Robert E W Hancock
Journal:  Biochim Biophys Acta       Date:  2016-10-18

4.  LvHemB1, a novel cationic antimicrobial peptide derived from the hemocyanin of Litopenaeus vannamei, induces cancer cell death by targeting mitochondrial voltage-dependent anion channel 1.

Authors:  Shangjie Liu; Jude Juventus Aweya; Liyuan Zheng; Zhou Zheng; He Huang; Fan Wang; Defu Yao; Tong Ou; Yueling Zhang
Journal:  Cell Biol Toxicol       Date:  2021-02-25       Impact factor: 6.691

5.  KIF21A regulates breast cancer aggressiveness and is prognostic of patient survival and tumor recurrence.

Authors:  Anton J Lucanus; Aye Aye Thike; Xing Fei Tan; Kee Wah Lee; Shiyuan Guo; Victoria P C King; Von Bing Yap; Boon Huat Bay; Puay Hoon Tan; George W Yip
Journal:  Breast Cancer Res Treat       Date:  2021-10-26       Impact factor: 4.872

6.  Pleurocidin-family cationic antimicrobial peptides are cytolytic for breast carcinoma cells and prevent growth of tumor xenografts.

Authors:  Ashley L Hilchie; Carolyn D Doucette; Devanand M Pinto; Aleksander Patrzykat; Susan Douglas; David W Hoskin
Journal:  Breast Cancer Res       Date:  2011-10-24       Impact factor: 6.466

Review 7.  The Human Cathelicidin Antimicrobial Peptide LL-37 and Mimics are Potential Anticancer Drugs.

Authors:  Kengo Kuroda; Kazuhiko Okumura; Hiroshi Isogai; Emiko Isogai
Journal:  Front Oncol       Date:  2015-06-30       Impact factor: 6.244

8.  Predicting sulfotyrosine sites using the random forest algorithm with significantly improved prediction accuracy.

Authors:  Zheng Rong Yang
Journal:  BMC Bioinformatics       Date:  2009-10-29       Impact factor: 3.169

Review 9.  Heparan sulfate and heparanase as modulators of breast cancer progression.

Authors:  Angélica M Gomes; Mariana P Stelling; Mauro S G Pavão
Journal:  Biomed Res Int       Date:  2013-07-31       Impact factor: 3.411

10.  Increased EXT1 gene copy number correlates with increased mRNA level predicts short disease-free survival in hepatocellular carcinoma without vascular invasion.

Authors:  Sheng Dong; Yifeng Wu; Shigang Yu; Yinxi Yang; Lijun Lu; Shurong Fan
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.889

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