Bluesky Facebook Reddit Email

Predicting resistance to brain tumor chemotherapy

12.12.11 | JCI Journals

Apple iPhone 17 Pro

Apple iPhone 17 Pro delivers top performance and advanced cameras for field documentation, data collection, and secure research communications.

Glioblastoma multiforme (GBM) is the most common and lethal of all human brain tumors that originate in the brain. For most patients, treatment involves surgery followed by both radiation therapy and chemotherapy with temozolomide. However, many GBMs are resistant to the effects of temozolomide. A team of researchers led by Sameer Agnihotri, at the University of Toronto, Toronto, has now determined that the protein APNG can contribute to GBM resistance to the effects of temozolomide. Importantly, high levels of expression of APNG in the nucleus of ressected tumor cells correlated with poorer overall survival compared with patients lacking APNG expression. Agnihotri, and colleagues therefore suggest that monitoring APNG levels could provide insight into whether or not a patient with GBM will respond to temozolomide, although this awaits confirmation in predictive and prospective studies.

TITLE: Alkylpurine–DNA–N-glycosylase confers resistance to temozolomide in xenograft models of glioblastoma multiforme and is associated with poor survival in patients

AUTHOR CONTACT:
Sameer Agnihotri
Hospital for Sick Children Research Institute, University of
Toronto, Toronto, Ontario, Canada.
Phone: 416-813-6688; Fax: 416-813-8456; E-mail: sameer.agnihotri@utoronto.ca .

Journal of Clinical Investigation

Keywords

Article Information

Contact Information

How to Cite This Article

APA:
JCI Journals. (2011, December 12). Predicting resistance to brain tumor chemotherapy. Brightsurf News. https://www.brightsurf.com/news/L556MMRL/predicting-resistance-to-brain-tumor-chemotherapy.html
MLA:
"Predicting resistance to brain tumor chemotherapy." Brightsurf News, Dec. 12 2011, https://www.brightsurf.com/news/L556MMRL/predicting-resistance-to-brain-tumor-chemotherapy.html.