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Genome-Wide Screening in Haploid Stem Cells Reveals Synthetic Lethality Targeting MLH1 and TP53 Deficient Tumours
Rivki Cashman1, Guy Haim-Abadi2, Elyad Lezmi1,2
1NewStem LTD, Jerusalem, Israel.
Abstract:
Synthetic lethality is defined as a type of genetic interaction where the combination of two genetic events results in cell death, whereas each of them separately does not. Synthetic lethality can be a useful tool in personalised oncology. MLH1 is a cancer-related gene that has a central role in DNA mismatch-repair and TP53 is the most frequently mutated gene in cancer. To identify genetic events that can lead to tumour death once either MLH1 or TP53 is mutated, a genome-wide genetic screening was performed. Thus, mutations in all protein-coding genes were introduced into haploid human embryonic stem cells (hESCs) with and without loss-of-function mutations in the MLH1 or TP53 genes. These experiments uncovered a list of putative hits with EXO1, NR5A2, and PLK2 genes for MLH1, and MYH10 gene for TP53 emerging as the most promising candidates. Synthetic lethal interactions of these genes were validated genetically or chemically using small molecules that inhibit these genes. The specific effects of SR1848, which inhibits NR5A2, ON1231320 or BI2536, which inhibits PLK2, and blebbistatin, which inhibits MYH10, were further validated in cancer cell lines. Finally, animal studies with CCL xenografts showed the selective effect of the small molecule BI2536 on MLH1-null tumours and of blebbistatin on TP53-mutated tumours. Thus, demonstrating their potential for personalised medicine, and the robustness of genetic screening in haploid hESCs in the context of cancer therapeutics.
Insights
Synthetic lethality exploits cancer vulnerabilities by combining genetic events to induce cell death. This study identifies new synthetic lethal partners for MLH1 and TP53 mutations, offering potential personalized cancer therapies.
Area of Science:
- Cancer Biology
- Genetics
- Pharmacology
Background:
- Synthetic lethality is a promising strategy for targeted cancer therapy.
- MLH1 and TP53 are critical cancer-related genes frequently altered in tumors.
- Identifying synthetic lethal interactions can reveal novel therapeutic targets.
Purpose of the Study:
- To discover genes that induce synthetic lethality when mutated alongside MLH1 or TP53.
- To validate these synthetic lethal interactions using small molecule inhibitors.
- To assess the therapeutic potential of identified targets in preclinical cancer models.
Main Methods:
- Genome-wide genetic screening in haploid human embryonic stem cells (hESCs).
- Introduction of loss-of-function mutations in MLH1 or TP53.
- Validation of synthetic lethal interactions using genetic and chemical approaches.
- Preclinical testing of small molecule inhibitors in cancer cell lines and xenograft models.
Main Results:
- Identified EXO1, NR5A2, and PLK2 as synthetic lethal partners for MLH1.
- Identified MYH10 as a synthetic lethal partner for TP53.
- Demonstrated selective killing of MLH1-null tumors with BI2536 (PLK2 inhibitor).
- Showcased selective killing of TP53-mutated tumors with blebbistatin (MYH10 inhibitor).
Conclusions:
- This study reveals novel synthetic lethal interactions for MLH1 and TP53.
- The identified targets and small molecules show potential for personalized cancer medicine.
- Genome-wide screening in haploid hESCs is a robust approach for cancer therapeutic discovery.

