Cisplatin‐Resistant CD44+ Lung Cancer Cells Are Sensitive to Auger Electrons

Karina Lindbøg Madsen, Poul Flemming Høilund-Carlsen, Oke Gerke, Birgitte Brinkmann Olsen

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Cancer stem cells (CSCs) are resistant to conventional therapy and present a major clinical challenge since they are responsible for the relapse of many cancers, including non-small cell lung cancer (NSCLC). Hence, future successful therapy should also eradicate CSCs. Auger electrons have demonstrated promising therapeutic potential and can induce DNA damage while sparing surrounding cells. Here, we sort primary patient-derived NSCLC cells based on their expression of the CSC-marker CD44 and investigate the effects of cisplatin and a thymidine analog (deoxyuridine) labeled with an Auger electron emitter (125I). We show that the CD44+ populations are more resistant to cisplatin than the CD44− populations. Interestingly, incubation with the thymidine analog 5-[125I]iodo-2′-deoxyuridine ([125I]I-UdR) induces equal DNA damage, G2/M cell cycle arrest, and apoptosis in the CD44− and CD44+ populations. Our results suggest that Auger electron emitters can also eradicate resistant lung cancer CD44+ populations.
Translated title of the contributionCisplatin-resistente CD44+ lunge kræft celler er sensitive overfor Auger elektroner
Original languageEnglish
JournalInternational Journal of Molecular Sciences
Volume23
Number of pages17
ISSN1661-6596
DOIs
Publication statusPublished - 27 Jun 2024

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