» Articles » PMID: 19921751

Notch Promotes Radioresistance of Glioma Stem Cells

Overview
Journal Stem Cells
Date 2009 Nov 19
PMID 19921751
Citations 325
Authors
Affiliations
Soon will be listed here.
Abstract

Radiotherapy represents the most effective nonsurgical treatments for gliomas. However, gliomas are highly radioresistant and recurrence is nearly universal. Results from our laboratory and other groups suggest that cancer stem cells contribute to radioresistance in gliomas and breast cancers. The Notch pathway is critically implicated in stem cell fate determination and cancer. In this study, we show that inhibition of Notch pathway with gamma-secretase inhibitors (GSIs) renders the glioma stem cells more sensitive to radiation at clinically relevant doses. GSIs enhance radiation-induced cell death and impair clonogenic survival of glioma stem cells but not non-stem glioma cells. Expression of the constitutively active intracellular domains of Notch1 or Notch2 protect glioma stem cells against radiation. Notch inhibition with GSIs does not alter the DNA damage response of glioma stem cells after radiation but rather reduces Akt activity and Mcl-1 levels. Finally, knockdown of Notch1 or Notch2 sensitizes glioma stem cells to radiation and impairs xenograft tumor formation. Taken together, our results suggest a critical role of Notch signaling to regulate radioresistance of glioma stem cells. Inhibition of Notch signaling holds promise to improve the efficiency of current radiotherapy in glioma treatment.

Citing Articles

Deciphering the Role of Cancer Stem Cells: Drivers of Tumor Evolution, Therapeutic Resistance, and Precision Medicine Strategies.

El-Tanani M, Rabbani S, Satyam S, Rangraze I, Wali A, El-Tanani Y Cancers (Basel). 2025; 17(3).

PMID: 39941751 PMC: 11815874. DOI: 10.3390/cancers17030382.


Regulatory role of circular RNAs in the development of therapeutic resistance in the glioma: A double-edged sword.

Masoomabadi N, Gorji A, Ghadiri T, Ebrahimi S Iran J Basic Med Sci. 2025; 28(1):3-15.

PMID: 39877636 PMC: 11771335. DOI: 10.22038/ijbms.2024.81644.17669.


Inflammasome activation in melanoma progression: the latest update concerning pathological role and therapeutic value.

Pluetrattanabha N, Direksunthorn T, Ahmad I, Jyothi S, Shit D, Singh A Arch Dermatol Res. 2025; 317(1):258.

PMID: 39820618 DOI: 10.1007/s00403-025-03802-1.


The Role of HDAC6 in Glioblastoma Multiforme: A New Avenue to Therapeutic Interventions?.

Spallotta F, Illi B Biomedicines. 2024; 12(11).

PMID: 39595195 PMC: 11591585. DOI: 10.3390/biomedicines12112631.


Harnessing the role of aberrant cell signaling pathways in glioblastoma multiforme: a prospect towards the targeted therapy.

Hasan S, Mahmud Z, Hossain M, Islam S Mol Biol Rep. 2024; 51(1):1069.

PMID: 39424705 DOI: 10.1007/s11033-024-09996-3.


References
1.
Bao S, Wu Q, McLendon R, Hao Y, Shi Q, Hjelmeland A . Glioma stem cells promote radioresistance by preferential activation of the DNA damage response. Nature. 2006; 444(7120):756-60. DOI: 10.1038/nature05236. View

2.
Zhang X, Zheng G, Zou L, Liu H, Hou L, Zhou P . Notch activation promotes cell proliferation and the formation of neural stem cell-like colonies in human glioma cells. Mol Cell Biochem. 2007; 307(1-2):101-8. DOI: 10.1007/s11010-007-9589-0. View

3.
Dotto G . Notch tumor suppressor function. Oncogene. 2008; 27(38):5115-23. PMC: 2747622. DOI: 10.1038/onc.2008.225. View

4.
Wang J, Chao J, Chen W, Kuo M, Yen J . The antiapoptotic gene mcl-1 is up-regulated by the phosphatidylinositol 3-kinase/Akt signaling pathway through a transcription factor complex containing CREB. Mol Cell Biol. 1999; 19(9):6195-206. PMC: 84561. DOI: 10.1128/MCB.19.9.6195. View

5.
Bao S, Wu Q, Sathornsumetee S, Hao Y, Li Z, Hjelmeland A . Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor. Cancer Res. 2006; 66(16):7843-8. DOI: 10.1158/0008-5472.CAN-06-1010. View