The ‘little blue pill’ may strengthen a newly discovered cholesterol-regulating mechanism that could be harnessed to curb cancer spread.
Cholesterol is particularly important for cancer cells seeking to break away from the primary tumor, migrate throughout the body and invade distant organs.
Elevated cGMP levels dilate blood vessels, increasing blood flow to the penis – the effect that has made Viagra a successful treatment for erectile dysfunction.
As a result, less cholesterol is available for the cell’s needs, and cancer cells, it turns out, are particularly vulnerable to this reduction in cholesterol supply.
The combination could not only limit cancer cells’ access to existing cholesterol but also prevent them from producing new cholesterol, potentially enhancing the anti-metastatic effect.
Original story from the Weizmann Institute of Science (Rehovot, Israel).
The ‘little blue pill’ may strengthen a newly discovered cholesterol-regulating mechanism that could be harnessed to curb cancer spread.
Viagra was originally developed to treat high blood pressure and chest pain caused by reduced blood flow to the heart, but over the past three decades it has become the world’s best-known therapy for erectile dysfunction. In the future, this blockbuster drug may find yet another use. In a study published recently in Cancer Research, scientists in the lab of Ayelet Erez at the Weizmann Institute of Science (Rehovot, Israel) found that sildenafil, Viagra’s active ingredient, may restrict cancer metastasis through a newly discovered biological mechanism.
The researchers, led by Yarden Ariav in Erez’s lab, showed that sildenafil limits cancer cells’ ability to make use of cholesterol, an essential component of cellular membranes. Cholesterol is particularly important for cancer cells seeking to break away from the primary tumor, migrate throughout the body and invade distant organs. When their access to cholesterol is disrupted, these cells have a harder time forming metastases.
Sildenafil creates this disruption by blocking an enzyme called phosphodiesterase type 5, or PDE5, thereby increasing the levels of a signaling molecule known as cGMP. Elevated cGMP levels dilate blood vessels, increasing blood flow to the penis – the effect that has made Viagra a successful treatment for erectile dysfunction. But Erez’s team discovered that cGMP also binds to a protein responsible for transporting cholesterol within cells. As a result, less cholesterol is available for the cell’s needs, and cancer cells, it turns out, are particularly vulnerable to this reduction in cholesterol supply.
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The researchers also found that combining drugs from the Viagra family with statins – another widely used class of drugs, which reduce cholesterol production in the body – may be even more effective at restricting metastasis. The combination could not only limit cancer cells’ access to existing cholesterol but also prevent them from producing new cholesterol, potentially enhancing the anti-metastatic effect.
The research team – which included scientists from the lab of Eytan Ruppin at the US National Cancer Institute (MD, USA), researchers from Clalit Health Services’ (Tel Aviv, Israel) Innovation Division led by Shay Ben-Shachar and physicians and scientists from Rabin Medical Center (Petah Tikva, Israel) – based its findings on mouse models of cancer, cultures of cancer cells from human patients and data collected over 20 years from some 5 million Clalit members. Consistent with the findings in mice and human cell cultures, statistical analysis of the Clalit database revealed significantly improved survival among cancer patients who took sildenafil, particularly when it was combined with statins.
“We have uncovered a new biological pathway that links a well-known signaling molecule to cholesterol regulation within cells, and shown how this pathway can be harnessed to interfere with the ability of cancer cells to form metastases,” explained Erez, who is also a practicing physician in addition to serving as a senior researcher and dean of Weizmann’s Miriam and Aaron Gutwirth Medical School. “Beyond their therapeutic promise, our findings highlight that cancer biology is shaped not only by mutations in tumor cells but also by the patient’s metabolic state and by medications they are already taking for other conditions.”
Erez added: “Our study underscores the importance of treating the whole patient – not just the cancer – when tailoring the most effective therapy.”
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