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Creation Date: 26 June 2012 | Review Date: 26 June 2012

Chemo Brain: The Fallout from Cancer Treatment

Source: Society for Neuroscience

For cancer patients, it’s a long haul from the time of diagnosis to the end of treatment. After numerous rounds of chemotherapy, patients feel relieved they survived and look forward to moving on. Unfortunately, however, another obstacle may stand in their way — a condition called chemo brain.

MRI scan shows decreases in gray matter after one month of chemotherapy, courtesy of Indiana University
An MRI scan shows decreases in gray matter in the brain's bilateral frontal lobes and cerebellum and right temporal lobe after one month of chemotherapy.
Courtesy of Indiana University

Chemo brain is a catch-all term for cognitive deficits following chemotherapy, a common cancer treatment where the body is treated with chemicals meant to kill fast-growing cells. People report short-term memory loss, difficulty retrieving information, problems switching from one task to another, and problems with attention.  

Scientists believe that chemotherapy-induced memory loss may be attributable to damage to the hippocampus, a brain structure vital to memory, while injury to the frontal lobe can lead to problems with cognitive function and control. More than 70 percent of patients find these difficulties subside several months after treatment ends, but at least one-fourth of that group continues to have these problems five and even ten years later. Women who have been treated with chemotherapy for breast cancer are particularly susceptible.

Vulnerable brain cells

Researchers have investigated these issues for more than a decade. In 2006, research from a team led by Mark Noble, professor at the University of Rochester Medical Center, revealed the extent of the problem: common chemotherapy drugs used to treat breast, ovarian, and colon and rectal cancer, as well as non-Hodgkin’s lymphoma, were more toxic to multiple kinds of brain cells than the cancer cells themselves. 

A later study by Noble’s team done in mice showed that another commonly used chemotherapeutic drug caused damage to oligodendrocytes, the cells that cover axons with myelin. Myelin helps expedite messaging among nerve cells, or neurons. When oligodendrocytes are damaged, myelin breaks down, disrupting communication among the nerve cells vital to brain functioning.     

Crossing the barrier between brain and body

Another team from the University of Rochester Medical Center hypothesized the drugs that cause chemo brain are those best able to cross the blood-brain barrier, a network of blood vessels that prevents more than 95 percent of all chemicals from entering the brain from the bloodstream. They tested this hypothesis by giving one group of mice a standard dose of cyclophosphamide and fluorouracil, which do cross into the brain, and a second group paclitaxel and doxorubicin, which do not. Surprisingly, all four drugs resulted in the breakdown of brain cells.  The largest reduction in brain cells came from paclitaxel  and cyclophosphamide (36 and 31 percent, respectively). Fluorouracil and doxorubicin produced lower reductions (15 and 22 percent, respectively).    

Robert Gross, a professor at the University of Rochester Medical Center and the study’s principal investigator, offered one possible explanation for these findings. “It could be that all of the chemo drugs cross into the brain after all, or that they act via peripheral mechanisms, such as inflammation, that could open up the blood-brain barrier.”  

Understanding the full impact

What can be done to offset these problems? Promising animal research at the University of Rochester suggests that the growth factor IGF-1 may help. When administered to mice under certain conditions — before and after receiving a single or multiple-dose regimen of cyclophosphamide — IGF-1 seemed to increase the number of new brain cells, although it did appear to be more effective in the high-dose model.  

“We’re still trying to understand the causes of chemo brain,” Gross said. “We plan to conduct additional studies to further test the impact of IGF-1 and other related interventions on the molecular and behavioral consequences of chemotherapy.” 

Further Reading

Davidson I. (20120).  Fighting the good fight against “chemo brain.” The Huffington Post.  Available at:

Dietrich J,  Han, R, Yang, Y, Mayer-Pröschel, M, and Noble, M. (2006). CNS progenitor cells and oligodendrocytes are targets of chemotherapeutic agents in vitro and in vivo. J. Biol. 5, e22.

Duffner PK. (2005)  Minireview: The long term effects of chemotherapy on the central nervous system. Journal of Biology 5:21. Available at:

Kesler S, Kent J, and O’Hara  R.(2011). Prefrontal cortex and executive functioning  impairments  in primary breast cancer. Archives of Neurology  68: 1447-1453.

Scherling C, Collins B, MacKenzie J, Bielajew C,  and Smith A. (2011).  Pre-chemotherapy differences in visuospatial working memory in breast cancer patients compared to controls: An fMRI study.  Frontiers in Human Neuroscience 5:122.    

University of Rochester  Newsroom (2009).  UR study reveals chemo’s toxicity to brain, possible treatment. Available at:

Winocur G et al.The effects of chemotherapy on cognitive function in a mouse model: A prospective study. Clinical Cancer Research  2012.  Available at:

About the Author

Marilyn Fenichel, freelance writer for the Society for Neuroscience, the American Academy for the Advancement of Science, and the National Science Foundation, among others.
Marilyn Fenichel served as the managing editor of the seventh edition of Brain Facts. She is a seasoned writer and editor and has worked for many organizations, including the National Science Foundation, the National Academies, and the American Association for the Advancement of Science.
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