Gliomas 2021
DOI: 10.36255/exonpublications.gliomas.2021.chapter4
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Emerging Roles of Wild-type and Mutant IDH1 in Growth, Metabolism and Therapeutics of Glioma

Abstract: Glioblastoma is one of the most devastating human malignancies and is categorized into primary and secondary glioblastoma subtypes that develop through different genetic pathways. Isocitrate dehydrogenase 1 (IDH1) and 2 (IDH2) are key enzymes linking cellular metabolism to epigenetic regulation and redox states. Hot spot mutations of IDH1 is early and frequent genetic alterations in secondary glioblastoma as well as in grade II and III glioma and represent a major biomarker with diagnostic, prognostic, and pre… Show more

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Cited by 7 publications
(7 citation statements)
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“…Mutations in the IDH enzyme worsen the prognosis of gliomas. It is therefore important to distinguish between the two types of glial tumor in order to tailor treatments and improve prognosis [27].…”
Section: Resultsmentioning
confidence: 99%
“…Mutations in the IDH enzyme worsen the prognosis of gliomas. It is therefore important to distinguish between the two types of glial tumor in order to tailor treatments and improve prognosis [27].…”
Section: Resultsmentioning
confidence: 99%
“…Glioblastomas with IDH-1 mutations account for 73% of tumors and are reported to have a slightly better prognosis due to their enhanced response to radiotherapy and temozolomide (26). Regardless, IDH-1 mutants and wildtype tumors have different metabolic profiles, suggesting that each type may have unique therapeutic vulnerabilities (27). One such potential vulnerability is seen in the IDH1 R132H mutational subtype, which has significantly improved prognosis versus other gliomas, and overexpresses microRNA mIR-128.…”
Section: Treatment Planningmentioning
confidence: 99%
“…Ang(1-7) binds to Mas receptors (MasRs) [117,118]. ATI may also be cleaved by ACE2 to form Ang (1)(2)(3)(4)(5)(6)(7)(8)(9), which can be cleaved by ACE1 and is converted to Ang(1-7), which in addition to binding to MasRs, can also bind to AT2R with low affinity, and Mas-related-G protein coupled receptors (MrgDs) [119]. MrgDs are a recently discovered component of the RAS [102], and their role in the GB TME is yet to be defined.…”
Section: The Renin-angiotensin System and Convergent Signaling Pathways In Glioblastomamentioning
confidence: 99%
“…IDH-wild-type GB is more common, tends to arise de novo, and is generally more aggressive with a worse prognosis than IDH-mutant GB. By contrast, IDH-mutant GB is predominantly observed in secondary GB and is associated with a better prognosis [6]. The current standard treatment for GB involves maximal safe surgical resection with adjuvant chemotherapy and radiotherapy, known as the Stupp protocol [7].…”
Section: Introductionmentioning
confidence: 99%