| Literature DB >> 35441348 |
Alison R Mercer-Smith1, Andrew Buckley1, Alain Valdivia1, Wulin Jiang1, Morrent Thang1, Noah Bell1, Rashmi J Kumar2, Hunter N Bomba1, Alex S Woodell1, Jie Luo3, Scott R Floyd3, Shawn D Hingtgen4,5.
Abstract
The spread of non-small cell lung cancer (NSCLC) to the leptomeninges is devastating with a median survival of only a few months. Radiation offers symptomatic relief, but new adjuvant therapies are desperately needed. Spheroidal, human induced neural stem cells (hiNeuroS) secreting the cytotoxic protein, TRAIL, have innate tumoritropic properties. Herein, we provide evidence that hiNeuroS-TRAIL cells can migrate to and suppress growth of NSCLC metastases in combination with radiation. In vitro cell tracking and post-mortem tissue analysis showed that hiNeuroS-TRAIL cells migrate to NSCLC tumors. Importantly, isobolographic analysis suggests that TRAIL with radiation has a synergistic cytotoxic effect on NSCLC tumors. In vivo, mice treated with radiation and hiNeuroS-TRAIL showed significant (36.6%) improvements in median survival compared to controls. Finally, bulk mRNA sequencing analysis showed both NSCLC and hiNeuroS-TRAIL cells showed changes in genes involved in migration following radiation. Overall, hiNeuroS-TRAIL cells +/- radiation have the capacity to treat NSCLC metastases.Entities:
Keywords: Cell-based drug delivery; Induced neural stem cells; Non-small cell lung cancer; Radiation
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Year: 2022 PMID: 35441348 DOI: 10.1007/s12015-022-10375-3
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 6.692