Literature DB >> 27573048

Current treatments for advanced melanoma and introduction of a promising novel gene therapy for melanoma (Review).

Jae-Rim Heo1, Nam-Hyung Kim2, Jaejin Cho3, Kyung-Chul Choi1.   

Abstract

Metastatic melanoma is a fatal form of skin cancer that has a tendency to proliferate more rapidly than any other solid tumor. Since 2010, treatment options for metastatic melanoma have been developed including chemotherapies, checkpoint inhibition immunotherapies, e.g., anti‑cytotoxic T‑lymphocyte antigen‑4 (CTLA‑4) and anti‑programmed death‑1 (PD‑1), and molecular-targeted therapies, e.g., BRAF and MEK inhibitors. These treatments have shown not only high response rates yet also side‑effects and limitations. Notwithstanding its limitations, stem cell therapy has emerged as a new auspicious therapy for various tumor types. Since stem cells possess the ability to serve as a novel vehicle for delivering therapeutic or suicide genes to primary or metastatic cancer sites, these cells can function as part of gene‑directed enzyme prodrug therapy (GDEPT). This review focuses on introducing engineered neural stem cells (NSCs), which have tumor‑tropic behavior that allows NSCs to selectively approach primary and invasive tumor foci, as a potential gene therapy for melanoma. Therapy using engineered NSCs with cytotoxic agents resulted in markedly reduced tumor volumes and significantly prolonged survival rates in preclinical models of various tumor types. This review elucidates current treatment options for metastatic melanoma and introduces a promising NSC therapy.

Entities:  

Mesh:

Year:  2016        PMID: 27573048     DOI: 10.3892/or.2016.5032

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  6 in total

1.  [Construction and verification of anti-MM scFv-tP fusion protein expression vector].

Authors:  Hao Wang; Yi-Fei Yang; Wei Wang; Bing Guan; Meng Xun; Hai Zhang; Zi-Ling Wang; Yong Zhao
Journal:  Nan Fang Yi Ke Da Xue Xue Bao       Date:  2017-09-20

2.  Resveratrol induced reactive oxygen species and endoplasmic reticulum stress‑mediated apoptosis, and cell cycle arrest in the A375SM malignant melanoma cell line.

Authors:  Jae-Rim Heo; Soo-Min Kim; Kyung-A Hwang; Ji-Houn Kang; Kyung-Chul Choi
Journal:  Int J Mol Med       Date:  2018-06-15       Impact factor: 4.101

3.  Curcumin plays a synergistic role in combination with HSV-TK/GCV in inhibiting growth of murine B16 melanoma cells and melanoma xenografts.

Authors:  Hong Li; Haiyan Du; Guangxian Zhang; Yingya Wu; Pengxiang Qiu; Jingjing Liu; Jing Guo; Xijuan Liu; Lingling Sun; Biaoyan Du; Yuhui Tan
Journal:  PeerJ       Date:  2019-09-20       Impact factor: 2.984

4.  A Potential Therapy Using Engineered Stem Cells Prevented Malignant Melanoma in Cellular and Xenograft Mouse Models.

Authors:  Jae-Rim Heo; Kyung-A Hwang; Seung U Kim; Kyung-Chul Choi
Journal:  Cancer Res Treat       Date:  2018-09-14       Impact factor: 4.679

Review 5.  Emergent Nanotechnological Strategies for Systemic Chemotherapy against Melanoma.

Authors:  Jacinta Oliveira Pinho; Mariana Matias; Maria Manuela Gaspar
Journal:  Nanomaterials (Basel)       Date:  2019-10-13       Impact factor: 5.076

Review 6.  Elucidation of Melanogenesis Cascade for Identifying Pathophysiology and Therapeutic Approach of Pigmentary Disorders and Melanoma.

Authors:  Tokimasa Hida; Takafumi Kamiya; Akinori Kawakami; Jiro Ogino; Hitoshi Sohma; Hisashi Uhara; Kowichi Jimbow
Journal:  Int J Mol Sci       Date:  2020-08-25       Impact factor: 5.923

  6 in total

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