Natural products targeting cancer cell dependency

被引:9
作者
Shi, Changxiang [1 ]
Yang, Eun Ju [1 ]
Tao, Shishi [1 ]
Ren, Guowen [1 ]
Mou, Pui Kei [1 ]
Shim, Joong Sup [1 ,2 ]
机构
[1] Univ Macau, Fac Hlth Sci, Ctr Canc, Taipa, Macao, Peoples R China
[2] Univ Macau, MoE Frontiers Sci Ctr Precis Oncol, Taipa, Macao, Peoples R China
关键词
KINASE-C-THETA; NITIDINE CHLORIDE; SYNTHETIC LETHALITY; NONACTIN BIOSYNTHESIS; AEROBIC GLYCOLYSIS; PRECISION MEDICINE; PROSTATE-CANCER; BREAST-CANCER; DNA-REPAIR; IN-VITRO;
D O I
10.1038/s41429-021-00438-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Precision cancer medicine is a tailored treatment approach for individual cancer patients with different genomic characteristics. Mutated or hyperactive oncogenes have served as main drug targets in current precision cancer medicine, while defective or inactivated tumor suppressors in general have not been considered as druggable targets. Synthetic lethality is one of very few approaches that enable to target defective tumor suppressors with pharmacological agents. Synthetic lethality exploits cancer cell dependency on a protein or pathway, which arises when the function of a tumor suppressor is defective. This approach has been proven to be effective in clinical settings since the successful clinical introduction of BRCA-PARP synthetic lethality for the treatment of breast and ovarian cancer with defective BRCA. Subsequently, large-scale screenings with RNAi, CRISPR/Cas9-sgRNAs, and chemical libraries have been applied to identify synthetic lethal partners of tumor suppressors. Natural products are an important source for the discovery of pharmacologically active small molecules. However, little effort has been made in the discovery of synthetic lethal small molecules from natural products. This review introduces recent advances in the discovery of natural products targeting cancer cell dependency and discusses potentials of natural products in the precision cancer medicine.
引用
收藏
页码:677 / 686
页数:10
相关论文
共 118 条
[1]   (-)-Englerin A is a Potent and Selective Activator of TRPC4 and TRPC5 Calcium Channels [J].
Akbulut, Yasemin ;
Gaunt, Hannah J. ;
Muraki, Katsuhiko ;
Ludlow, Melanie J. ;
Amer, Mohamed S. ;
Bruns, Alexander ;
Vasudev, Naveen S. ;
Radtke, Lea ;
Willot, Matthieu ;
Hahn, Sven ;
Seitz, Tobias ;
Ziegler, Slava ;
Christmann, Mathias ;
Beech, David J. ;
Waldmann, Herbert .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2015, 54 (12) :3787-3791
[2]   Targeting BRCA1-BER deficient breast cancer by ATM or DNA-PKcs blockade either alone or in combination with cisplatin for personalized therapy [J].
Albarakati, Nada ;
Abdel-Fatah, Tarek M. A. ;
Doherty, Rachel ;
Russell, Roslin ;
Agarwal, Devika ;
Moseley, Paul ;
Perry, Christina ;
Arora, Arvind ;
Alsubhi, Nouf ;
Seedhouse, Claire ;
Rakha, Emad A. ;
Green, Andrew ;
Ball, Graham ;
Chan, Stephen ;
Caldas, Carlos ;
Ellis, Ian O. ;
Madhusudan, Srinivasan .
MOLECULAR ONCOLOGY, 2015, 9 (01) :204-217
[3]   Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial [J].
Audeh, M. William ;
Carmichael, James ;
Penson, Richard T. ;
Friedlander, Michael ;
Powell, Bethan ;
Bell-McGuinn, Katherine M. ;
Scott, Clare ;
Weitzel, Jeffrey N. ;
Oaknin, Ana ;
Loman, Niklas ;
Lu, Karen ;
Schmutzler, Rita K. ;
Matulonis, Ursula ;
Wickens, Mark ;
Tutt, Andrew .
LANCET, 2010, 376 (9737) :245-251
[4]   Inhibition of AKT suppresses the initiation and progression of BRCA1-associated mammary tumors [J].
Baek, Hye Jung ;
Kim, Sun Eui ;
Kim, Jong Kwang ;
Shin, Dong Hoon ;
Kim, Tae Hyun ;
Kim, Kwang Gi ;
Deng, Chu-Xia ;
Kim, Sang Soo .
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2018, 14 (13) :1769-1781
[5]   Englerin A induces an acute inflammatory response and reveals lipid metabolism and ER stress as targetable vulnerabilities in renal cell carcinoma [J].
Batova, Ayse ;
Altomare, Diego ;
Creek, Kim E. ;
Naviaux, Robert K. ;
Wang, Lin ;
Li, Kefeng ;
Green, Erica ;
Williams, Richard ;
Naviaux, Jane C. ;
Diccianni, Mitchell ;
Yu, Alice L. .
PLOS ONE, 2017, 12 (03)
[6]   A high-throughput screen to identify novel synthetic lethal compounds for the treatment of E-cadherin-deficient cells [J].
Beetham, Henry ;
Chen, Augustine ;
Telford, Bryony J. ;
Single, Andrew ;
Jarman, Kate E. ;
Lackovic, Kurt ;
Luxenburger, Andreas ;
Guilford, Parry .
SCIENTIFIC REPORTS, 2019, 9 (1)
[7]   Prioritization of cancer therapeutic targets using CRISPR-Cas9 screens [J].
Behan, Fiona M. ;
Iorio, Francesco ;
Picco, Gabriele ;
Goncalves, Emanuel ;
Beaver, Charlotte M. ;
Migliardi, Giorgia ;
Santos, Rita ;
Rao, Yanhua ;
Sassi, Francesco ;
Pinnelli, Marika ;
Ansari, Rizwan ;
Harper, Sarah ;
Jackson, David Adam ;
Mcrae, Rebecca ;
Pooley, Rachel ;
Wilkinson, Piers ;
van der Meer, Dieudonne ;
Dow, David ;
Buser-Doepner, Carolyn ;
Bertotti, Andrea ;
Trusolino, Livio ;
Stronach, Euan A. ;
Saez-Rodriguez, Julio ;
Yusa, Kosuke ;
Garnett, Mathew J. .
NATURE, 2019, 568 (7753) :511-+
[8]   Precision medicine in gastric cancer [J].
Bonelli, Patrizia ;
Borrelli, Antonella ;
Tuccillo, Franca Maria ;
Silvestro, Lucrezia ;
Palaia, Raffaele ;
Buonaguro, Franco Maria .
WORLD JOURNAL OF GASTROINTESTINAL ONCOLOGY, 2019, 11 (10) :804-829
[9]   Biological activities of nitidine, a potential antimalarial lead compound [J].
Bouquet, Jerome ;
Rivaud, Marion ;
Chevalley, Severine ;
Deharo, Eric ;
Jullian, Valerie ;
Valentin, Alexis .
MALARIA JOURNAL, 2012, 11
[10]   Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase [J].
Bryant, HE ;
Schultz, N ;
Thomas, HD ;
Parker, KM ;
Flower, D ;
Lopez, E ;
Kyle, S ;
Meuth, M ;
Curtin, NJ ;
Helleday, T .
NATURE, 2005, 434 (7035) :913-917