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Synthetic lethality and DNA damage response targeting in cancer stem cells: a comprehensive review

Usamah SayedFaculty of Allied Medical Sciences, Hourani Center for Applied Scientific Research, Al-Ahliyya Amman University, Amman, JordanWaleed K. AbdulsahibDepartment of Pharmacology and Toxicology, College of Pharmacy, Al Farahidi University, Baghdad, Iraq. [email protected]Ihsan Khudhair JasimDepartment of Pharmaceutics, Faculty of Pharmacy, Al-Turath University, Baghdad, IraqH. MalathiDepartment of Biotechnology and Genetics, School of Sciences, JAIN (Deemed to be University), Bangalore, Karnataka, IndiaPriya Priyadarshini NayakDepartment of Medical Oncology, IMS and SUM Hospital, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, 751003, Odisha, IndiaD. Alex AnandDepartment of Biomedical, Sathyabama Institute of Science and Technology, Chennai, Tamil Nadu, IndiaGunjan MukherjeeUniversity Institute of Biotechnology, Chandigarh University, Mohali, Punjab, IndiaAashna SinhaSchool of Applied and Life Sciences, Division of Research and Innovation, Uttaranchal University, Dehradun, Uttarakhand, IndiaSadridin EshkaraevDepartment of Medicine, Termez University of Economics and Serviсe, Termez, Uzbekistan
Discover Oncologyjournal2026en
ABI

Аннотация

This comprehensive review explores the critical intersection of Synthetic Lethality (SL) and DNA Damage Response (DDR) targeting within Cancer Stem Cells (CSCs), a subpopulation central to tumor initiation, metastasis, and therapeutic resistance. CSCs exhibit unique biological properties, including enhanced DNA repair mechanisms and metabolic plasticity, rendering them intrinsically resistant to conventional therapies. The fundamental mechanisms of DDR pathways and their dysregulation in cancer are delineated, highlighting how these vulnerabilities can be exploited through SL. The review synthesizes current preclinical and clinical advancements in targeting CSCs via DDR inhibitors, including PARP, ATR, ATM, and DNA-PKcs inhibitors, as well as emerging SL targets. Furthermore, advanced therapeutic modalities such as small molecule inhibitors, antibody-drug conjugates, CAR cell therapies, glycan-based approaches, and nanoparticle delivery systems tailored for CSC elimination are discussed. Finally, persistent challenges, including CSC heterogeneity, the immunosuppressive tumor microenvironment, on-target/off-tumor toxicities, and translational hurdles, are addressed, emphasizing the transformative potential of integrated diagnostic platforms leveraging AI, liquid biopsy, multi-omics, and single-cell profiling to usher in a new era of precision oncology for durable cancer control.

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Показатели — AkademScholar · Скоро