Therapeutics to prevent cisplatin-induced hearing loss by transcriptomics
Therapeutics to prevent cisplatin-induced hearing loss by transcriptomics
批准号:
10007294
负责人:
Pezhman Salehi Dermanaki
金额:
$20.57万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-04-01 至 2021-09-30
关键词:
Animal ModelAuditory Brainstem ResponsesAuditory ThresholdBioinformaticsBlood - brain barrier anatomyCancer PatientCell Culture TechniquesCell LineCellsCisplatinCochleaDatabasesDoseDose-LimitingDrug or ChemicalFVB MouseFreedomGenomicsGoalsGrantHair CellsHead CancerIn VitroInjectionsIntraperitoneal InjectionsInvestigational TherapiesLabyrinthLegal patentLicensingMalignant NeoplasmsMalignant neoplasm of lungMalignant neoplasm of ovaryMapsModelingMorphologyMusNatureNeck CancerNeuronsOrgan of CortiOrphan DrugsPathway interactionsPatientsPharmaceutical PreparationsPharmacotherapyPhasePhenotypePlatinumPortraitsPrincipal InvestigatorProcessPublishingReportingResistanceSensoryStria VascularisTestingTherapeuticTimeUnited States Food and Drug AdministrationUniversitiesWorkZebrafishauditory threshold shiftbasecancer cellcancer therapychemotherapycisplatin induced hearing losscostcytotoxicitydrug candidatehearing impairmentin vivoin vivo Modelintraperitoneallateral linemouse modelnephrotoxicityneuromastneurotoxicitynovelnovel therapeuticsotoprotectantototoxicitypermanent hearing losspre-clinicalpreventprevent hearing lossside effectspiral gangliontranscriptometranscriptome sequencingtranscriptomicsweb-based tool
中文摘要
转录组学预防顺铂性听力损失的治疗方法
英文摘要
Therapeutics to prevent cisplatin-induced hearing loss by transcriptomics
PROJECT SUMMARY
Cisplatin is one of the most effective platinum-based compounds in the treatment of various types
of malignancies, including head and neck, ovarian, and lung cancer. Despite its efficacy, ototoxcity,
neurotoxicity, and nephrotoxicity stand out as the top three dose-limiting side effects of cisplatin
chemotherapy.
Ototoxicity refers to drug or chemical-related damage to the inner ear sensory cells and neurons,
resulting in permanent, irreversible hearing loss. Elevation of hearing thresholds have been reported
in the majority of patients treated with cisplatin. To date, there are no FDA-approved drugs for the
treatment of cisplatin-induced hearing loss.
This study aims to prevent cisplatin-induced damage to the inner ear cells by investigating drug
candidates which activate multiple pathways involved in mechanisms of cisplatin resistance. Using
recent advances in developing bioinformatic web-based tools that integrate genomic portraits and
compound activities, we have identified 6 FDA-approved candidate drugs that could be associated
with a cisplatin-resistant phenotype. The 6 final top drugs were selected based on their FDA-approval
and ability to grant at least 40% protection in either cellular or zebrafish models. The drug providing
the highest protection in cell culture, zebrafish and cochlear explant models has also been shown to
have synergistic effects on cisplatin in cancer cells and can cross the blood-brain-barrier. Therefore,
the combination of its protective nature in cochlear cells and destructive nature in cancer cells makes
it a viable option as a drug for cisplatin resistance for the inner ear.
The results of this study will provide the key proof of principle to develop novel therapeutic
strategies against side effects of cisplatin chemotherapy. Moreover, our studies will provide
mechanisms of action of cisplatin-induced hearing loss. Repurposing this FDA-approved drug for new
function against the side-effects of cisplatin chemotherapy will significantly expedite the FDA approval
process and reduce its cost.
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