logo

Characterization of ALDH1A1 Positive Cancer Stem Cells in Glioblastoma Multiforme and Their Response to Temozolomide

Authors
  • Bhoomika Patel

    Sumandeep Nursing College, Sumandeep Vidyapeeth (Deemed to be University), Vadodara, Gujarat, India
  • Rucha N. Acharya

    Faculty of Allied and Healthcare, Gokul Global University, Sidhpur, Gujarat, India
  • Prakhar Goyal

    Quantum University Research Center, Quantum University, Roorkee, Uttarakhand, 247667, India
  • Lalatendu Moharana

    Department of Onco-Medicine, IMS and SUM Hospital, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, Odisha, India
  • B. Senthil Kumar

    Department of Anatomy, Vinayaka Mission’s Kirupananda Variyar Medical College & Hospitals, Vinayaka Mission’s Research Foundation (DU), Salem, Tamil Nadu, India
  • Takveer Singh

    Centre for Research Impact & Outcome, Chitkara University Institute of Engineering and Technology, Chitkara University, Rajpura, 140401, Punjab, India
  • S. Renuka Jyothi

    Department of Biotechnology and Genetics, JAIN (Deemed-to-be University), Bengaluru, Karnataka, India
Keywords:
Glioblastoma Multiforme, ALDH1A1, Cancer Stem Cells, Temozolomide Resistance, Tumor Heterogeneity, Stemness Markers, Targeted Cancer Therapy
Abstract

Glioblastoma multiforme (GBM) is a type of primary brain cancer that is associated with high malignancy and cellular diversity, along with a poor response to traditional treatment approaches. The function of ALDH1A1 has been linked with stem cell-like properties and drug resistance in various types of cancers. This research focuses on studying the stem cell-like properties and sensitivity to temozolomide (TMZ) of ALDH1A1-positive groups of cells in GBM cell lines. Human GBM cell lines, including U87-MG and U251, were grown and divided into ALDH1A1-positive and ALDH1A1-negative fractions by ALDEFLUOR test and flow cytometry. TMZ resistance was determined by means of the MTT test and apoptosis assay. ALDH1A1-positive cells comprised about 33.2 ± X% of the examined sample (n = X). As compared to ALDH1A1-negative cells, ALDH1A1-positive cells displayed increased ability to form spheres, high expression levels of stem-like markers, and decreased susceptibility to the effects of TMZ. At 48 hours of exposure to TMZ, cells expressing ALDH1A1 had a higher level of viability compared to those not expressing it. This shows a relationship between ALDH1A1 and the stem-cell characteristics of the GBM cells. There is a need for further research in this field with the use of patient samples and manipulation of ALDH1A1.

Downloads
Download data is not yet available.
References

[1] Jiménez R, Constantinescu A, Yazir M, Alfonso-Triguero P, Pequerul R, Parés X, Lorenzo J. Targeting Retinaldehyde Dehydrogenases to Enhance Temozolomide Therapy in Glioblastoma. International Journal of Molecular Sciences 2024; 25(21): 11512.

[2] Lim JR, Mouawad J, Gorton OK, Bubb WA, Kwan AH. Cancer stem cell characteristics and their potential as therapeutic targets. Medical Oncology 2021; 38(7): 76.

[3] Wei P, Jiang J, Xiao M, Zeng M, Liu X, Zhao B, Chen F. The transcript ENST00000444125 of lncRNA LINC01503 promotes cancer stem cell properties of glioblastoma cells via reducing FBXW1-mediated GLI2 degradation. Experimental Cell Research 2022; 412(1): 113009.

[4] Magrassi L, Pinton G, Luzzi S, Comincini S, Scravaglieri A, Gigliotti V, Garavaglia S. A new vista of aldehyde dehydrogenase 1A3 (ALDH1A3): new specific inhibitors and activity-based probes targeting ALDH1A3-dependent pathways in glioblastoma, mesothelioma, and other cancers. Cancers 2024; 16(13): 2397.

[5] Gelardi EL, Caprioglio D, Colombo G, Del Grosso E, Mazzoletti D, Mattoteia D, Garavaglia S. Curcumin-based fluorescent probes targeting ALDH1A3 as a promising tool for glioblastoma precision surgery and early diagnosis. Communications Biology 2022; 5(1): 895.

[6] Nandhinieswari S, Indumathi A. Bilevel optimized recursive feature eliminator for cervical cancer feature selection process. Archives for Technical Sciences 2024; 2(31): 311-328.

[7] Liu A, Yu X, Liu S. Pluripotency transcription factors and cancer stem cells: small genes make a big difference. Chinese Journal of Cancer 2013; 32(9): 483.

[8] Bamodu OA, Chung CC, Pisanic TR, Wu AT. The intricate interplay between cancer stem cells and cell-of-origin of cancer: implications for therapeutic strategies. Frontiers in Oncology 2024; 14: 1404628.

[9] Xu H, Si Q, Song Y, Sun S, Wei X, Long H, Wang X. Cancer stem cell heterogeneity-inspired therapeutics for enhancing tumor treatment outcomes. International Journal of Oncology 2025; 68(2): 18.

[10] Samanta K, Reddy GSVSR, Sharma NK, Kar P. Deciphering the role of functional ion channels in cancer stem cells (CSCs) and their therapeutic implications. International Journal of Molecular Sciences 2025; 26(15): 7595.

[11] Zhang S, Yang R, Ouyang Y, Shen Y, Hu L, Xu C. Cancer stem cells: a target for overcoming therapeutic resistance and relapse. Cancer Biology & Medicine 2023; 20(12): 985-1020.

[12] Nguyen AL, Facey CO, Boman BM. The significance of aldehyde dehydrogenase 1 in cancers. International Journal of Molecular Sciences 2024; 26(1): 251.

[13] Castelli V, Giordano A, Benedetti E, Giansanti F, Quintiliani M, Cimini A, d’Angelo M. The great escape: the power of cancer stem cells to evade programmed cell death. Cancers 2021; 13(2): 328.

[14] Guo L, Yan T, Guo W, Niu J, Wang W, Ren T, Wang B. Molecular subtypes of osteosarcoma classified by cancer stem cell related genes define immunological cell infiltration and patient survival. Frontiers in Immunology 2022; 13: 986785.

[15] Mehta A, Singh RK. Targeting Tumor Microenvironment in Metastatic Cancer. In Medxplore: Frontiers in Medical Science. Periodic Series in Multidisciplinary Studies 2025; pp. 1-18.

[16] Sharma A, Nair V. Developing a Medical Coding Curriculum for Surgery Students by Resolving Inconsistencies among Physician and Student Records. Global Journal of Medical Terminology Research and Informatics 2025; 2(1): 30-36.

[17] Wu L, Katsube T, Li X, Wang B, Xie Y. Unveiling the impact of CD133 on cell cycle regulation in radio-and chemoresistance of cancer stem cells. Frontiers in Public Health 2025; 13: 1509675.

[18] Jahangiri L, Ishola T, Pucci P, Trigg RM, Pereira J, Williams JA, Turner SD. The role of autophagy and lncRNAs in the maintenance of cancer stem cells. Cancers 2021; 13(6): 1239.

[19] Kudaravalli S, den Hollander P, Mani SA. Role of p38 MAP kinase in cancer stem cells and metastasis. Oncogene 2022; 41(23): 3177-3185.

[20] Swain N, Thakur M, Pathak J, Swain B. SOX2, OCT4 and NANOG: The core embryonic stem cell pluripotency regulators in oral carcinogenesis. Journal of Oral and Maxillofacial Pathology: JOMFP 2020; 24(2): 368.

Downloads
Published
30-09-2026
Section
Articles

How to Cite

Characterization of ALDH1A1 Positive Cancer Stem Cells in Glioblastoma Multiforme and Their Response to Temozolomide. (2026). Journal of Cancer Research Updates, 15(3), 328-337. https://doi.org/10.30683/1929-2279.2026.15.29

Similar Articles

1-10 of 257

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)