LOS ANGELES (Dec. 13, 2024) — A new study from Cedars-Sinai Cancer reveals a potential way to overcome tumor resistance to a common chemotherapy drug called cisplatin.
The study, published in the peer-reviewed journal Science Advances, could improve the effectiveness of the widely used platinum-based medication and reduce the required dosage, minimizing side effects.
“We found that by inhibiting the action of a gene that limits the importation of the drug into tumor cells, we can increase the uptake of cisplatin and thus its effectiveness,” said Dan Theodorescu, MD, PhD, director of Cedars-Sinai Cancer, the PHASE ONE Foundation Distinguished Chair, and co-senior author of the study. “This gives us a druggable target to enhance patient response, especially in cases of advanced disease, and we have demonstrated this in multiple cancer types. We hope these findings will make cisplatin therapy more effective and an option for more patients.”
Cisplatin is widely used as part of first-line therapy for many cancer types, including bladder, ovarian, cervical, testicular, lung and breast cancer, as well as sarcomas, lymphomas and leukemias. Nearly 50% of all patients who receive chemotherapy receive platinum-based drugs, which work by damaging the DNA of tumor cells to prevent them from multiplying. However, tumor cells are often able to “escape” the drugs’ effects, so these therapies rarely cure advanced disease.
To explore ways to overcome cancer cells’ resistance to cisplatin, investigators from Cedars-Sinai, the University of Colorado Anschutz Medical Campus, and Erasmus University Medical Center, Rotterdam, The Netherlands, worked with bladder cancer cells in laboratory mice and in cell culture, and also with organoids grown from patients’ bladder cancer cells. Tumor organoids are clusters of cells, grown in a petri dish, that share many characteristics with actual tumors.
“We showed that inhibition of a gene called NPEPPS increased sensitivity to cisplatin in these cells and organoids, providing the first description of this gene’s role in cisplatin resistance,” Theodorescu said. “Our data have shown the importance of this pathway in various cancer types and in patients who had platinum-based therapy. Our data have clearly identified NPEPPS as a promising target for drug development for patients with treatment-resistant cancer.”
Previous research has shown that platinum-based chemotherapy used along with immunotherapy can improve immunotherapy effectiveness, which further broadens the impact of these findings, Theodorescu said.
“All cells have channels that sit on the cell surface and control what goes in and out of the cell. It turns out that some of these channels import platinum drugs into cells,” said James Costello, PhD, associate professor of Pharmacology at University of Colorado Anschutz Medical Campus and co-senior author of the study. “What we discovered in this study is that NPEPPS is the protein that gets turned up in response to platinum drugs and it blocks the channels that import platinum drugs. So, by targeting NPEPPS therapeutically, we can prevent it from blocking these channels. We are continuing to study how blocking NPEPPS therapeutically affects both tumor and normal cells, including interactions with the immune system.”
Ongoing studies are aimed at more fully understanding how NPEPPS inhibits the import of cisplatin into cancer cells and at discovering drugs that can inhibit NPEPPS. Combining these drugs with cisplatin would make the cisplatin more effective at killing cancer cells, leading to better patient outcomes.
Additional Cedars-Sinai authors: Saswat Mohapatra, Fangyuan Qu, Corazon Gutierrez, Huihui Ye, Sarah Parker
Additional authors: Lily Elizabeth R Feldman, Robert T Jones, Charlene B Tilton, Michael V Orman, Molishree Joshi, Cailin S Deiter, Eric T Clambey, James C Costello, Mathijs Scholtes, Tokameh Mahmoudi, Tahlita Zuiverloon, Travis P Broneske
Funding: Anschutz Foundation to J.C.C., CA268055 to J.C.C. and D.T., Pharmacology T32 Training Grant GM007635 supported L.E.F., Cancer Center Shared Resources, NIH NCI CA046934
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