» Articles » PMID: 26972863

Neurocognitive Functioning and Genetic Variation in Patients with Primary Brain Tumours

Overview
Journal Lancet Oncol
Specialty Oncology
Date 2016 Mar 15
PMID 26972863
Citations 37
Authors
Affiliations
Soon will be listed here.
Abstract

Impairment of neurocognitive functioning is a common result of cerebral neoplasms and treatment, although there is substantial heterogeneity in the pattern and severity of neurocognitive dysfunction across individuals and tumour types. The effects of many clinical and patient characteristics on neurocognitive functioning have been documented, but little research has been devoted to understanding the effect of genetic variation on neurocognitive outcomes in patients with brain tumours. This Review highlights preliminary evidence that suggests an association between various genes and risk of adverse neurocognitive outcomes in patients with brain tumours. Studies include genes specific to neuronal function, and those associated with more systemic cellular regulation. Related scientific literature in other disease populations is briefly discussed to indicate additional candidate genes. We consider methodological issues central to the study of neurocognitive functioning and genetic associations for patients with brain tumours, and emphasise the need for future research integrating novel investigative techniques.

Citing Articles

ICAM-1 and IL-10 are associated with cognitive dysfunction using the MoCA test in glioma: Findings from the NCI Neuro-Oncology Branch Natural History Study.

Slattery K, Kauss M, Raval D, Hsieh E, Choi A, Davis T Neurooncol Adv. 2025; 7(1):vdaf002.

PMID: 40041201 PMC: 11879401. DOI: 10.1093/noajnl/vdaf002.


Glioblastoma-derived migrasomes promote migration and invasion by releasing PAK4 and LAMA4.

Huang Z, Wang M, Chen Y, Tang H, Tang K, Zhao M Commun Biol. 2025; 8(1):91.

PMID: 39833606 PMC: 11747271. DOI: 10.1038/s42003-025-07526-w.


The value of systemic immune inflammation index, white blood cell to platelet ratio, and homocysteine in predicting the instability of small saccular intracranial aneurysms.

Zhang W, Xiang C, Liu B, Hou F, Zheng Z, Chen Z Sci Rep. 2024; 14(1):24312.

PMID: 39414876 PMC: 11484959. DOI: 10.1038/s41598-024-74870-y.


Neuropsychological Evaluation for Oncology.

Sheppard D, Noll K, Wefel J, Bradshaw M Neurol Clin. 2024; 42(4):875-887.

PMID: 39343481 PMC: 11443061. DOI: 10.1016/j.ncl.2024.05.012.


Understanding treatment preferences and cognitive outcomes in patients with gliomas.

Succop Jr B, Richardson D, Rauf Y, Higgins D, Catalino M Support Care Cancer. 2024; 32(10):673.

PMID: 39292365 DOI: 10.1007/s00520-024-08876-7.


References
1.
Brackett J, Krull K, Scheurer M, Liu W, Srivastava D, Stovall M . Antioxidant enzyme polymorphisms and neuropsychological outcomes in medulloblastoma survivors: a report from the Childhood Cancer Survivor Study. Neuro Oncol. 2012; 14(8):1018-25. PMC: 3408256. DOI: 10.1093/neuonc/nos123. View

2.
Waterhouse E, An J, Orefice L, Baydyuk M, Liao G, Zheng K . BDNF promotes differentiation and maturation of adult-born neurons through GABAergic transmission. J Neurosci. 2012; 32(41):14318-30. PMC: 3519245. DOI: 10.1523/JNEUROSCI.0709-12.2012. View

3.
Lio D, Annoni G, Licastro F, Crivello A, Forte G, Scola L . Tumor necrosis factor-alpha -308A/G polymorphism is associated with age at onset of Alzheimer's disease. Mech Ageing Dev. 2006; 127(6):567-71. DOI: 10.1016/j.mad.2006.01.015. View

4.
Ostrom Q, Gittleman H, Liao P, Rouse C, Chen Y, Dowling J . CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2007-2011. Neuro Oncol. 2014; 16 Suppl 4:iv1-63. PMC: 4193675. DOI: 10.1093/neuonc/nou223. View

5.
Lecomte T, Landi B, Beaune P, Laurent-Puig P, Loriot M . Glutathione S-transferase P1 polymorphism (Ile105Val) predicts cumulative neuropathy in patients receiving oxaliplatin-based chemotherapy. Clin Cancer Res. 2006; 12(10):3050-6. DOI: 10.1158/1078-0432.CCR-05-2076. View