Use of existing, well-established hypertension drugs could improve the outcome of cancer chemotherapy by opening up collapsed blood vessels in solid tumors. In their report in the online journal Nature Communications,
Massachusetts General Hospital (MGH) investigators describe how the
angiotensin inhibitor losartan improved the delivery of chemotherapy
drugs and oxygen throughout tumors by increasing blood flow in mouse
models of breast and pancreatic cancer. A clinical trial based on the findings of this study is now underway.
"Angiotensin inhibitors are safe blood pressure medications that have
been used for over a decade in patients and could be repurposed for
cancer treatment," explains Rakesh K. Jain, PhD, director of the Steele
Laboratory for Tumor Biology at MGH and senior author of the study.
"Unlike anti-angiogenesis drugs, which improve tumor
blood flow by repairing the abnormal structure of tumor blood vessels,
angiotensin inhibitors open up those vessels by releasing physical
forces that are applied to tumor blood vessels when the gel-like matrix
surrounding them expands with tumor growth."
Focusing on how the physical and physiological properties of tumors can
inhibit cancer therapies, Jain's team previously found that losartan
improves the distribution within tumors of relatively large molecules
called nanomedicines by inhibiting the formation of collagen, a primary
constituent of the extracellular matrix. The current study looked at
whether losartan and other drugs that block the action of angiotensin - a
hormone with many functions in the body - could release the elevated
forces within tumors that compress and collapse internal blood vessels.
These stresses are exerted when cancer-associated fibroblasts (CAFs) -
specialized cells in the tumor microenvironment - proliferate and
produce increased levels of both collagen and a gel-like substance
called hyaluronan.
The team's experiments in several mouse models showed that both collagen
and hyaluronan are involved in the compression of blood vessels within
tumors and that losartan inhibited production of both molecules by CAFs
through reducing the activation and overall density of these cells.
Compared with drugs called ACE inhibitors, which block angiotensin
signaling in a different way, losartan and drugs of its class - termed
angiotensin receptor blockers - appeared better at reducing compression
within tumors. In models of breast and pancreatic cancer, treatment with
losartan alone had little effect on tumor growth, but combining
losartan with standard chemotherapy drugs delayed the growth of tumors
and extended survival.
"Increasing tumor blood flow in the absence of anti-cancer drugs might
actually accelerate tumor growth, but we believe that combining
increased blood flow with chemotherapy, radiation therapy or
immunotherapy will have beneficial results," explains Jain, the Cook
Professor of Radiation Oncology (Tumor Biology) at Harvard Medical
School. "Based on these findings in animal models, our colleagues at the
MGH Cancer Center have initiated a clinical trial to test whether
losartan can improve treatment outcomes in pancreatic cancer."
Information on this trial is available here.
No comments:
Post a Comment