Synthetic lethality on drug discovery: an update on cancer therapy

被引:15
|
作者
Yar, M. Shahar [1 ]
Haider, Kashif [1 ]
Gohel, Vivek [2 ]
Siddiqui, Nasir Ali [3 ]
Kamal, Ahmed [1 ]
机构
[1] Jamia Hamdard, Sch Pharmaceut Educ & Res, Dept Pharmaceut Chem, New Delhi 110062, India
[2] NIPER SAS Nagar, Dept Pharmacol & Toxicol, Mohali, India
[3] King Saud Univ, Coll Pharm, Riyadh, Saudi Arabia
关键词
Synthetic lethality; PARP; BRCA; cancer; METASTATIC COLORECTAL-CANCER; DEPENDENT PROTEIN-KINASE; HOMOLOGY-DIRECTED REPAIR; DNA-DAMAGE RESPONSE; BRCA MUTANT-CELLS; POLY(ADP-RIBOSE) POLYMERASE; PARP INHIBITOR; STRAND BREAKS; MYC; ACTIVATION;
D O I
10.1080/17460441.2020.1744560
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: A novel anticancer therapy is the need of the hour due to growing incidences of resistance to first line cancer chemotherapy. Synthetic lethality (SL) is one of the new age treatment methods being explored for combating the resistance to anticancer agents. In this method, cell mutations are exploited for the development of new therapeutic agents, where, if there is loss of function of one gene, the cell mutations can still be fixed by alternative machinery but if two genes involved in DNA repair undergo loss of function, it causes lethality to the cell. Areas covered: The authors condense findings of SL-based novel anticancer regimen. The review emphasizes some of the SL based clinical and preclinical studies of novel targets and therapy. Expert opinion: SL conceptualizes a resolution against treatment resistance to anticancer regimen by recognition of therapeutic vulnerabilities in particular cancer cells. A multitude of clinical trials associated with SL and DNA repair are being conducted that will be useful in obtaining a clearer picture pertaining to the use of cancer biomarkers and effectiveness of drugs acting via target-based molecular changes. Furthermore, new anticancer regimen focused on personalized medicines will emerge basing their development upon SL.
引用
收藏
页码:823 / 832
页数:10
相关论文
共 50 条
  • [1] Synthetic lethality as an engine for cancer drug target discovery
    Alan Huang
    Levi A. Garraway
    Alan Ashworth
    Barbara Weber
    [J]. Nature Reviews Drug Discovery, 2020, 19 : 23 - 38
  • [2] Synthetic lethality as an engine for cancer drug target discovery
    Huang, Alan
    Garraway, Levi A.
    Ashworth, Alan
    Weber, Barbara
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2020, 19 (01) : 23 - 38
  • [3] A lethal combination for cancer cells: Synthetic lethality screenings for drug discovery
    Ferrari, Elisa
    Lucca, Chiara
    Foiani, Marco
    [J]. EUROPEAN JOURNAL OF CANCER, 2010, 46 (16) : 2889 - 2895
  • [4] An update on small molecule compounds targeting synthetic lethality for cancer therapy
    Luo, Jiaxiang
    Li, Yang
    Zhang, Yiwen
    Wu, Defa
    Ren, Yijiu
    Liu, Jie
    Wang, Chengdi
    Zhang, Jifa
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2024, 278
  • [5] Methylation synthetic lethality: Exploiting selective drug targets for cancer therapy
    Ye, Bing-Jie
    Li, Di-Fei
    Li, Xin-Yun
    Hao, Jia-Lin
    Liu, Di-Jie
    Yu, Hang
    Zhang, Chun- Dong
    [J]. CANCER LETTERS, 2024, 597
  • [6] Synthetic lethality in personalized cancer therapy
    Ying Pang
    Meng Cheng
    Mu Chen
    Kaijun Zhao
    Yuanyuan Yin
    Min Liu
    Jing Zhang
    Chunlong Zhong
    [J]. Genome Instability & Disease, 2023, 4 (2) : 121 - 135
  • [7] Metabolic synthetic lethality in cancer therapy
    Zecchini, Vincent
    Frezza, Christian
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2017, 1858 (08): : 723 - 731
  • [8] What's next for the synthetic lethality drug discovery engine?
    Mullard, Asher
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (07) : 477 - 479
  • [9] What’s next for the synthetic lethality drug discovery engine?
    Asher Mullard
    [J]. Nature Reviews Drug Discovery, 2022, 21 : 477 - 479
  • [10] Synthetic Lethality to Overcome Cancer Drug Resistance
    Porcelli, L.
    Quatrale, A. E.
    Mantuano, P.
    Silvestris, N.
    Brunetti, A. E.
    Calvert, H.
    Paradiso, A.
    Azzariti, A.
    [J]. CURRENT MEDICINAL CHEMISTRY, 2012, 19 (23) : 3858 - 3873