Literature DB >> 26374366

Temozolomide for Treating Malignant Melanoma.

Rong-Hua Li1, Xiao-Yang Hou1, Chun-Sheng Yang2, Wen-Lou Liu1, Jian-Qin Tang1, Yan-Qun Liu1, Guan Jiang1.   

Abstract

Melanoma is one of the most malignant forms of skin cancer; with a rapidly increasing prevalence. Early-stage melanoma is curable, but advanced metastatic melanoma is almost always fatal, and patients with such advanced disease have short median survival. Surgery and radiotherapy play a limited role in the treatment of metastatic melanoma. Rather, chemotherapy remains the mainstay of treatment, although other approaches, including biotherapy and gene therapy, have been attempted. The authors hereby, evaluated the use of temozolomide (TMZ) for treating metastatic melanoma compared to dacarbazine (DTIC), the effectiveness of TMZ for treating brain metastases, as well as TMZ resistance and how the efficacy of TMZ in malignant melanoma can be increased. Two chemotherapeutic regimens are commonly used for palliative treatment of malignant melanoma: intravenous administration of DTIC and oral administration of the alkylating agent temozolomide (TMZ). Compared to DTIC, TMZ is very well tolerated and has an advantage in terms of improving the quality of life of patients with metastatic melanoma. While the prognosis is currently unpromising, chemotherapy plays a palliative role for patients with metastatic melanoma. The toxicity of treatment regimens based on DTIC and TMZ do not differ significantly, although TMZ is costlier. These findings provide a reference for future researchers via a comprehensive analysis of the relevant literature.

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Year:  2015        PMID: 26374366     DOI: 09.2015/JCPSP.680688

Source DB:  PubMed          Journal:  J Coll Physicians Surg Pak        ISSN: 1022-386X            Impact factor:   0.711


  5 in total

1.  Dipotassium Glycyrrhizinate on Melanoma Cell Line: Inhibition of Cerebral Metastases Formation by Targeting NF-kB Genes-Mediating MicroRNA-4443 and MicroRNA-3620-Dipotassium Glycyrrhizinate Effect on Melanoma.

Authors:  Gabriel Alves Bonafé; Jéssica Silva Dos Santos; Jussara Vaz Ziegler; Fernando Augusto Lima Marson; Thalita Rocha; Manoela Marques Ortega
Journal:  Int J Mol Sci       Date:  2022-06-29       Impact factor: 6.208

2.  Effect of Lonidamine on Systemic Therapy of DB-1 Human Melanoma Xenografts with Temozolomide.

Authors:  Kavindra Nath; David S Nelson; Jeffrey Roman; Mary E Putt; Seung-Cheol Lee; Dennis B Leeper; Jerry D Glickson
Journal:  Anticancer Res       Date:  2017-07       Impact factor: 2.480

3.  Melanoma-associated mutants within the serine-rich domain of PAK5 direct kinase activity to mitogenic pathways.

Authors:  Kyle M LaPak; Dennis C Vroom; Ayush A Garg; Xiangnan Guan; John L Hays; Jonathan W Song; Christin E Burd
Journal:  Oncotarget       Date:  2018-05-22

4.  Revealing the epigenetic effect of temozolomide on glioblastoma cell lines in therapeutic conditions.

Authors:  Agnieszka Belter; Jakub Barciszewski; Anna-Maria Barciszewska
Journal:  PLoS One       Date:  2020-02-26       Impact factor: 3.240

5.  Long-Term Exposure to Temozolomide Affects Locomotor Activity and Cartilage Structure of Elderly Experimental Rats.

Authors:  Anastasia V Suhovskih; Olga P Molodykh; Victor S Ushakov; Maxim O Politko; Dmitry K Sokolov; Elena V Koldysheva; Elvira V Grigorieva
Journal:  Biomedicines       Date:  2020-11-26
  5 in total

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