A team of researchers, including UNC Lineberger’s Norman E. Sharpless, MD, has shown that chemotherapy triggers a pro-inflammatory stress response termed cellular senescence, promoting the adverse effects of chemotherapy as well as cancer relapse and metastasis. Eliminating the senescent cells in mice prevented the side effects and relapse.
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Standard chemotherapy is a blunt force instrument against cancer – and it’s a rare cancer patient who escapes debilitating side effects from systemic treatments that mostly affect dividing cells, both malignant and healthy, throughout the body. Researchers at the University of North Carolina Lineberger Comprehensive Cancer Center and their colleagues now show that chemotherapy triggers a pro-inflammatory stress response termed cellular senescence, promoting the adverse effects of chemotherapy as well as cancer relapse and metastasis. Eliminating the senescent cells in mice prevented the side effects and relapse. The research is published in Cancer Discovery.
“While chemotherapy does save lives, it often comes with a very high price,” said Judith Campisi, PhD, of the Buck Institute and senior scientist on the study. “Our work in mice studied the effects of chemotherapy on cancer relapse and other serious side effects. It provides a proof-of-principle that we hope can be translated into clinical practice.”
Campisi’s latest work highlights the two-faced nature of cellular senescence. It’s a biological mechanism that puts a break on cancer by permanently stopping stressed cells from dividing, but it also contributes to aging and late-life cancers. That’s because senescent cells are not benign – they secrete inflammatory molecules that damage neighboring tissues and cells. “Chemotherapy induces widespread senescence, contributing to persistent local and systemic inflammation,” Campisi said. “That’s why many patients feel so awful following treatment.”
The research, led by Marco Demaria, PhD, a former postdoc in the Campisi lab, utilized transgenic mice that permit tracking and eliminating senescent cells. Results showed that eliminating chemotherapy-induced senescent cells reduced several short-and long-term effects of treatment, including bone marrow suppression, toxicity to the heart, cancer recurrence and metastasis, and physical activity and strength. Common chemotherapy drugs Doxorubicin, Paclitaxel, Temozolomide and Cisplatin were used to treat the mice.
Demaria, who is now a principle investigator at the European Research Institute for the Biology of Ageing, at the University Medical Center, Groningen, Netherlands, said some of the most striking results involved running speed – an indicator of fatigue in mice. “Eliminating senescent cells was sufficient to almost entirely rescue the decline in physical activity in the treated mice,” he said. “Normally, mice spend 40 percent of their time running. After chemotherapy that activity dropped to 10 percent. When we knocked out the senescent cells the mice returned to normal running.”
“Fatigue, which can be long-lasting, is a big deal for patients on chemotherapy,” said UNC Lineberger Director Norman E. Sharpless, MD, and a co-author of the study, “Years later they often say that was the worst part of the treatment.”
“Chemotherapy-induced bone marrow injury can lead to reduction in blood cell production, which can contribute to chemotherapy-induced fatigue,” Said Daohong Zhou, MD, associate director for Basic Research of the Winthrop P. Rockefeller Cancer Institute at the University of Arkansas for Medical Sciences in Little Rock and a co-author of the study, “Eliminating senescent cells can promote bone marrow recovery after chemotherapy.”
Sharpless looked at blood markers of cellular senescence in 89 women with breast cancer before they underwent chemotherapy aimed at curing their disease. “Women who went into chemotherapy with the highest existing burden of senescent cells experienced the most debilitating fatigue after treatment,” he said. “It didn’t really matter what particular drug was used – the results following chemotherapy tracked to the existing burden of senescent cells.”
“We are excited about the potential applications of this work,” said Campisi. “It would be a huge benefit if we could reduce the risk of cancer relapse and metastasis in patients. We also think it would be great to mitigate the other side effects of chemotherapy, the fear of which sometimes keep patients from seeking treatment.”
Citation: Cellular senescence promotes adverse effects of chemotherapy and cancer relapse DOI: 10.1158/2159-8290.CD-16-0241.
The other researchers involved in the study include: Allison M Deal, Shani Alston and Hyman Muss from UNC Lineberger; Monique N. O’Leary, Su Liu, Fatouma Alimirah, Kristin Koenig, Catherine Le, Emmeline C. Academia, Sumner Kilmarx, Alexis Valdovinos, Brian K. Kennedy, and Simon Melov of the Buck; Boshi Wang from the European Institute for the Biology of Aging, University of Groningen, Netherlands; Jianhui Chang, Lijan Shao, and Daohong Zhou from the Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock; Natalia Mitin from HealthSpan Diagnostics, Research Triangle Park, North Carolina; and Alain de Bruin, Department of Pathobiology, University of Utrecht, Netherlands.
The work was supported by grants from the American Italian Cancer Foundation and the National Institutes of Health grants AG009909, AG017242, AG041122 and CA122023.
Campisi and Zhou are co-founders of Unity Biotechnology which is developing drugs to eliminate senescent cells. Sharpless and Demaria have equity in the company. Sharpless is a founder and has a financial interest in HealthSpan Diagnostics. Mitin is an employee of HealthSpan Diagnostics. All other authors declare no financial interests.