Literature DB >> 28322141

Lessons Learned from Gemcitabine: Impact of Therapeutic Carrier Systems and Gemcitabine's Drug Conjugates on Cancer Therapy.

Sathish Dyawanapelly1, Animesh Kumar2, Manish K Chourasia2.   

Abstract

Currently, drug delivery systems have a high impact in cancer therapy and are receiving more attention than conventional cancer treatment modalities. Compared with current cancer therapies, gemcitabine (2', 2'-difluoro-2'-deoxycytidine) has been proven to be an effective chemotherapeutic agent against pancreatic, colon, bladder, breast, ovarian, non-small-cell lung, and head and neck cancers in combination with other anticancer agents. To improve the safety and efficacy of cytotoxic drugs, several drug delivery systems have been explored. This review outlines the recent work directed toward gemcitabine delivery systems for cancer therapy, including aerosols, polymeric nanoparticles, liposomes, microparticles, carbon nanotubes, and multifunctional theranostic nanomedicines. It also provides insight into the design and development of gemcitabine conjugation for safe and effective cancer therapy. Despite the clinical promises of gemcitabine, many therapeutic challenges remain. Specifically, its therapeutic use in cancer chemotherapy is impeded by a short biological half-life, caused by its rapid metabolism, and resistance due to increased expression of ribonucleotide reductase. In our opinion, many research investigations have contributed to improve the selectivity and efficacy of gemcitabine. This combined approach of drug delivery systems and gemcitabine conjugates has shown promising efficacy in preclinical models and significant potential for future clinical cancer-therapeutic applications. Also, these strategies overcome most of the aforementioned limits of gemcitabine.

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Year:  2017        PMID: 28322141     DOI: 10.1615/CritRevTherDrugCarrierSyst.2017017912

Source DB:  PubMed          Journal:  Crit Rev Ther Drug Carrier Syst        ISSN: 0743-4863            Impact factor:   4.889


  5 in total

1.  Improving Plasma Stability and Bioavailability In Vivo of Gemcitabine Via Nanoparticles of mPEG-PLG-GEM Complexed with Calcium Phosphate.

Authors:  Wei Chu; Pengqian Tian; Ning Ding; Qing Cai; Jinlong Li; Xuezhi Zhuo; Zhaohui Tang; Jingxin Gou; Tian Yin; Yu Zhang; Haibing He; Xing Tang
Journal:  Pharm Res       Date:  2018-10-11       Impact factor: 4.200

2.  Retracted Article: Gemcitabine aggravates miR-199a-5p-mediated breast cancer cell apoptosis by promoting VEGFA downregulation via inactivating the AKT signaling pathway.

Authors:  Dingmei Deng; Xian Ye; Xiyue Wang; Guangning He
Journal:  RSC Adv       Date:  2019-07-01       Impact factor: 4.036

3.  Specific inhibitor of Notch‑3 enhances the sensitivity of NSCLC cells to gemcitabine.

Authors:  Bi-Dan Hu; Jia Guo; Yuan-Zi Ye; Ting Du; Chun-Song Cheng; Qian Jiang; Ruo-Nan Liu; Yan-Bei Zhang
Journal:  Oncol Rep       Date:  2018-05-16       Impact factor: 3.906

4.  miR-205-5p downregulation decreases gemcitabine sensitivity of breast cancer cells via ERp29 upregulation.

Authors:  Changpo Ma; Xuejun Shi; Wenchao Guo; Fukai Feng; Guangshun Wang
Journal:  Exp Ther Med       Date:  2019-08-30       Impact factor: 2.447

5.  Spironolactone, a Classic Potassium-Sparing Diuretic, Reduces Survivin Expression and Chemosensitizes Cancer Cells to Non-DNA-Damaging Anticancer Drugs.

Authors:  Tomomi Sanomachi; Shuhei Suzuki; Keita Togashi; Asuka Sugai; Shizuka Seino; Masashi Okada; Takashi Yoshioka; Chifumi Kitanaka; Masahiro Yamamoto
Journal:  Cancers (Basel)       Date:  2019-10-14       Impact factor: 6.639

  5 in total

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