A genetic roadmap to the response to genotoxic agents in human cells.
Alberto CicciaRoger A GreenbergSusan P Lees-MillerAndré NussenzweigPublished in: Faculty reviews (2022)
To maintain genome fidelity and prevent diseases such as cancer, our cells must constantly detect, and efficiently and precisely repair, DNA damage. Paradoxically, DNA-damaging agents in the form of radiation and chemotherapy are also used to treat cancer. Olivieri et al. used a CRISPR-based screen to identify genes that, when disrupted, lead to sensitivity or resistance to 27 different DNA-damaging agents used in the lab and/or in the clinic to treat cancer patients 1 . Their results reveal multiple new genes and connections that regulate these critical DNA damage repair pathways, with implications for basic and clinical research as well as cancer therapy.
Keyphrases
- genome wide
- dna damage
- papillary thyroid
- dna methylation
- cancer therapy
- oxidative stress
- squamous cell
- circulating tumor
- induced apoptosis
- dna repair
- single molecule
- cell free
- copy number
- high throughput
- gene expression
- squamous cell carcinoma
- genome wide identification
- signaling pathway
- nucleic acid
- transcription factor
- radiation induced
- cell cycle arrest
- endoplasmic reticulum stress
- genome editing
- pi k akt
- functional connectivity