Preclinical Synergistic Combination Therapy of Lurbinectedin with Irinotecan and 5-Fluorouracil in Pancreatic Cancer.
Tej TummalaAshley Sanchez Sevilla UruchurtuArielle De La CruzKelsey E HuntingtonAndrew GeorgeNicholas R LiguoriLeiqing ZhangLanlan ZhouAbbas E AbbasChristopher G AzzoliWafik S El-DeiryPublished in: Current oncology (Toronto, Ont.) (2023)
Pancreatic cancer is a devastating disease with a poor prognosis. Novel chemotherapeutics in pancreatic cancer have shown limited success, illustrating the urgent need for new treatments. Lurbinectedin (PM01183; LY-01017) received FDA approval in 2020 for metastatic small cell lung cancer on or after platinum-based chemotherapy and is currently undergoing clinical trials in a variety of tumor types. Lurbinectedin stalls and degrades RNA Polymerase II and introduces breaks in DNA, causing subsequent apoptosis. We now demonstrate lurbinectedin's highly efficient killing of human-derived pancreatic tumor cell lines PANC-1, BxPC-3, and HPAF-II as a single agent. We further demonstrate that a combination of lurbinectedin and irinotecan, a topoisomerase I inhibitor with FDA approval for advanced pancreatic cancer, results in the synergistic killing of pancreatic tumor cells. Western blot analysis of combination therapy indicates an upregulation of γH2AX, a DNA damage marker, and the Chk1/ATR pathway, which is involved in replicative stress and DNA damage response. We further demonstrate that the triple combination between lurbinectedin, irinotecan, and 5-fluorouracil (5-FU) results in a highly efficient killing of tumor cells. Our results are developing insights regarding molecular mechanisms underlying the therapeutic efficacy of a novel combination drug treatment for pancreatic cancer.
Keyphrases
- combination therapy
- highly efficient
- poor prognosis
- dna damage response
- small cell lung cancer
- dna damage
- clinical trial
- long non coding rna
- oxidative stress
- dna repair
- squamous cell carcinoma
- endothelial cells
- single molecule
- stem cells
- cancer therapy
- cell death
- emergency department
- signaling pathway
- mesenchymal stem cells
- open label
- water soluble
- brain metastases
- phase ii
- circulating tumor cells