Skip to playerSkip to main content
  • 1 week ago
Investigators at the Icahn School of Medicine at Mount Sinai have revealed that merely 5% of pancreatic cancer cells are capable of forming immune-suppressing environments that safeguard adjacent tumor cells. The findings, featured in Nature, highlighted the roles of PAI1 and PAI2 proteins in maintaining fibrin around tumors, which in turn attracts immune-suppressing macrophages and restricts the activity of cancer-fighting T cells. In experimental models, the elimination of either protein resulted in a reduction of tumor size by over 50%, and the combination of anti-PD-1 therapy with gene knockout nearly increased median survival from 24 to 47 days. Additional studies are required to evaluate the safety and efficacy of this strategy for patients.

Disclosure: This video contains stock footage and content created or enhanced using Al-assisted tools.
ai-generated

Category

🗞
News
Transcript
00:00Researchers at Mount Sinai have uncovered a surprising finding about pancreatic cancer.
00:05Just 5% of cancer cells may be enough to protect an entire tumor from immune attack.
00:10The study, published in Nature, focused on proteins called PAI1 and PAI2.
00:16These proteins help preserve fibrin, a material normally involved in blood clotting and wound repair.
00:22Around tumors, fibrin can create protected areas that attract immune-suppressing macrophages.
00:28That environment can keep cancer-fighting T-cells from reaching tumor cells effectively.
00:33In laboratory models, removing either PAI1 or PAI2 cut tumor burden by more than half.
00:39The altered tumors also showed more than twice as many CD8 T-cells.
00:44Researchers then combined the changes with anti-PD-1 immunotherapy.
00:48Median survival nearly doubled, increasing from 24 to 47 days in one mouse experiment.
00:54An experimental PAI1-blocking drug also improved survival when paired with immunotherapy.
01:00However, these treatment results were conducted in animals.
01:04Researchers say further studies are needed to determine whether this approach can safely help people with pancreatic cancer.

Recommended