Chemical genetic screens reveal defective lysosomal trafficking as synthetic lethal with NF1 loss.
Stephanie J BouleyAndrew V GrassettiRobert J AllawayMatthew D WoodHelen W HouIndia R Burdon DasbachWilliam L SeibelJimmy WuScott A GerberKonstantin H DragnevJames A WalkerYolanda SanchezPublished in: Journal of cell science (2024)
Neurofibromatosis type 1, a genetic disorder caused by pathogenic germline variations in NF1, predisposes individuals to the development of tumors, including cutaneous and plexiform neurofibromas (CNs and PNs), optic gliomas, astrocytomas, juvenile myelomonocytic leukemia, high-grade gliomas and malignant peripheral nerve sheath tumors (MPNSTs), which are chemotherapy- and radiation-resistant sarcomas with poor survival. Loss of NF1 also occurs in sporadic tumors, such as glioblastoma (GBM), melanoma, breast, ovarian and lung cancers. We performed a high-throughput screen for compounds that were synthetic lethal with NF1 loss, which identified several leads, including the small molecule Y102. Treatment of cells with Y102 perturbed autophagy, mitophagy and lysosome positioning in NF1-deficient cells. A dual proteomics approach identified BLOC-one-related complex (BORC), which is required for lysosome positioning and trafficking, as a potential target of Y102. Knockdown of a BORC subunit using siRNA recapitulated the phenotypes observed with Y102 treatment. Our findings demonstrate that BORC might be a promising therapeutic target for NF1-deficient tumors.
Keyphrases
- signaling pathway
- high grade
- induced apoptosis
- lps induced
- pi k akt
- high throughput
- oxidative stress
- nuclear factor
- cell cycle arrest
- small molecule
- genome wide
- peripheral nerve
- inflammatory response
- low grade
- cell proliferation
- cell death
- endoplasmic reticulum stress
- young adults
- toll like receptor
- single cell
- mass spectrometry
- blood brain barrier
- gene expression
- dna methylation
- optical coherence tomography
- risk assessment
- protein protein
- dna repair
- single molecule