Unravelling the Role of PARP1 in Homeostasis and Tumorigenesis: Implications for Anti-Cancer Therapies and Overcoming Resistance

被引:1
作者
Lovsund, Taylor [1 ]
Mashayekhi, Fatemeh [1 ]
Fitieh, Amira [2 ]
Stafford, James [3 ]
Ismail, Ismail Hassan [1 ,2 ]
机构
[1] Univ Alberta, Fac Med & Dent, Dept Oncol, Div Expt Oncol, 11560 Univ Ave, Edmonton, AB T6G 1Z2, Canada
[2] Cairo Univ, Fac Sci, Dept Biophys, Giza 12613, Egypt
[3] Univ Alberta, Fac Sci, Dept Biol Sci, Edmonton, AB T6G 2E1, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
genome instability; DNA repair; PARP1; PARPi resistance; PARylation; homologous recombination; NUCLEOTIDE EXCISION-REPAIR; RIBOSE POLYMERASE PARP; HOMOLOGOUS RECOMBINATION; SYNTHETIC LETHALITY; DNA-DAMAGE; HISTONE DEMETHYLASE; ADP-RIBOSYLATION; PROSTATE-CANCER; AP SITE; REPLICATION;
D O I
10.3390/cells12141904
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Detailing the connection between homeostatic functions of enzymatic families and eventual progression into tumorigenesis is crucial to our understanding of anti-cancer therapies. One key enzyme group involved in this process is the Poly (ADP-ribose) polymerase (PARP) family, responsible for an expansive number of cellular functions, featuring members well established as regulators of DNA repair, genomic stability and beyond. Several PARP inhibitors (PARPi) have been approved for clinical use in a range of cancers, with many more still in trials. Unfortunately, the occurrence of resistance to PARPi therapy is growing in prevalence and requires the introduction of novel counter-resistance mechanisms to maintain efficacy. In this review, we summarize the updated understanding of the vast homeostatic functions the PARP family mediates and pin the importance of PARPi therapies as anti-cancer agents while discussing resistance mechanisms and current up-and-coming counter-strategies for countering such resistance.
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页数:23
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