Sphingolipid/Ceramide Pathways and Autophagy in the Onset and Progression of Melanoma: Novel Therapeutic Targets and Opportunities

被引:33
|
作者
Lai, Michele [1 ]
La Rocca, Veronica [1 ]
Amato, Rachele [1 ]
Freer, Giulia [1 ]
Pistello, Mauro [1 ,2 ]
机构
[1] Univ Pisa, Dept Translat Res & New Technol Med & Surg, Retrovirus Ctr & Virol Sect, I-56127 Pisa, Italy
[2] Pisa Univ Hosp, Virol Unit, I-56127 Pisa, Italy
关键词
melanoma; sphingolipids; ceramides; acid ceramidase; multidrug resistance; autophagy; DAUNORUBICIN-INDUCED APOPTOSIS; ACID CERAMIDASE INHIBITORS; GLUCOSYLCERAMIDE SYNTHASE; POOR-PROGNOSIS; P-GLYCOPROTEIN; SPHINGOSINE; 1-PHOSPHATE; CELL-PROLIFERATION; GAUCHER-DISEASE; CANCER CELLS; EXPRESSION;
D O I
10.3390/ijms20143436
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melanoma is a malignant tumor deriving from neoplastic transformation of melanocytes. The incidence of melanoma has increased dramatically over the last 50 years. It accounts for most cases of skin cancer deaths. Early diagnosis leads to remission in 90% of cases of melanoma; conversely, for melanoma at more advanced stages, prognosis becomes more unfavorable also because dvanced melanoma is often resistant to pharmacological and radiological therapies due to genetic plasticity, presence of cancer stem cells that regenerate the tumor, and efficient elimination of drugs. This review illustrates the role of autophagy in tumor progression and resistance to therapy, focusing on molecular targets for future drugs.
引用
收藏
页数:15
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