NTPDase5/PCPH as a New Target in Highly Aggressive Tumors: A Systematic Review
Author(s) -
Paula A. Bracco,
Ana Paula Santin Bertoni,
Michaël Wink
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/123010
Subject(s) - systematic review , medicine , medline , bioinformatics , biology , computational biology , biochemistry
The protooncogene PCPH was recently identified as being the ectonucleoside triphosphate diphosphohydrolase 5 ( ENTPD5 ). This protooncogene is converted into an oncogene by a single base pair deletion, resulting in frame change and producing a premature stop codon, leading to a mutated protein (mt-PCPH) with only 27 kDa, which is much smaller than the original 47 kDa protein. Overexpression of the PCPH as well as the mutated PCPH increases the cellular resistance to stress and apoptosis. This is intriguing considering that the active form, that is, the oncogene, is the mutated PCPH. Several studies analyzed the expression of NTPDase5/mt-PCPH in a wide range of tumor cells and evaluated its role and mechanisms in cancer and other pathogenic processes. The main point of this review is to integrate the findings and proposed theories about the role played by NTPDase5/mt-PCPH in cancer progression, considering that these proteins have been suggested as potential early diagnostic tools and therapy targets.
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