Literature DB >> 34725718

Four decades of chemotherapy-induced cognitive dysfunction: comprehensive review of clinical, animal and in vitro studies, and insights of key initiating events.

Ana Dias-Carvalho1,2, Mariana Ferreira3,4,5, Rita Ferreira5, Maria de Lourdes Bastos3,4, Susana Isabel Sá6,7, João Paulo Capela3,4,8, Félix Carvalho3,4, Vera Marisa Costa9,10.   

Abstract

Cognitive dysfunction has been one of the most reported and studied adverse effects of cancer treatment, but, for many years, it was overlooked by the medical community. Nevertheless, the medical and scientific communities have now recognized that the cognitive deficits caused by chemotherapy have a strong impact on the morbidity of cancer treated patients. In fact, chemotherapy-induced cognitive dysfunction or 'chemobrain'  (also named also chemofog) is at present a well-recognized effect of chemotherapy that could affect up to 78% of treated patients. Nonetheless, its underlying neurotoxic mechanism is still not fully elucidated. Therefore, this work aimed to provide a comprehensive review using PubMed as a database to assess the studies published on the field and, therefore, highlight the clinical manifestations of chemobrain and the putative neurotoxicity mechanisms.In the last two decades, a great number of papers was published on the topic, mainly with clinical observations. Chemotherapy-treated patients showed that the cognitive domains most often impaired were verbal memory, psychomotor function, visual memory, visuospatial and verbal learning, memory function and attention. Chemotherapy alters the brain's metabolism, white and grey matter and functional connectivity of brain areas. Several mechanisms have been proposed to cause chemobrain but increase of proinflammatory cytokines with oxidative stress seem more relevant, not excluding the action on neurotransmission and cellular death or impaired hippocampal neurogenesis. The interplay between these mechanisms and susceptible factors makes the clinical management of chemobrain even more difficult. New studies, mainly referring to the underlying mechanisms of chemobrain and protective measures, are important in the future, as it is expected that chemobrain will have more clinical impact in the coming years, since the number of cancer survivors is steadily increasing.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Chemobrain; Chemofog; Chemotherapy; Cognitive impairment; Neurotoxicity

Mesh:

Substances:

Year:  2021        PMID: 34725718     DOI: 10.1007/s00204-021-03171-4

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  272 in total

1.  Neuropsychologic impact of standard-dose systemic chemotherapy in long-term survivors of breast cancer and lymphoma.

Authors:  Tim A Ahles; Andrew J Saykin; Charlotte T Furstenberg; Bernard Cole; Leila A Mott; Karen Skalla; Marie B Whedon; Sarah Bivens; Tara Mitchell; E Robert Greenberg; Peter M Silberfarb
Journal:  J Clin Oncol       Date:  2002-01-15       Impact factor: 44.544

2.  2-Mercaptoethane sulfonate prevents doxorubicin-induced plasma protein oxidation and TNF-α release: implications for the reactive oxygen species-mediated mechanisms of chemobrain.

Authors:  Christopher D Aluise; Sumitra Miriyala; Teresa Noel; Rukhsana Sultana; Paiboon Jungsuwadee; Tamara J Taylor; Jian Cai; William M Pierce; Mary Vore; Jeffrey A Moscow; Daret K St Clair; D Allan Butterfield
Journal:  Free Radic Biol Med       Date:  2011-03-21       Impact factor: 7.376

Review 3.  Candidate mechanisms for chemotherapy-induced cognitive changes.

Authors:  Tim A Ahles; Andrew J Saykin
Journal:  Nat Rev Cancer       Date:  2007-03       Impact factor: 60.716

4.  Ameliorative effect of metformin on cyclophosphamide-induced memory impairment in mice.

Authors:  A H Alhowail; S Chigurupati; S Sajid; V Mani
Journal:  Eur Rev Med Pharmacol Sci       Date:  2019-11       Impact factor: 3.507

5.  The effects of chemotherapy on Useful Field of View (UFOV) in younger and older breast cancer patients.

Authors:  Carolyn E Adams-Price; Linda W Morse; Ginger W Cross; Marsha Williams; Elisabeth Wells-Parker
Journal:  Exp Aging Res       Date:  2009 Apr-Jun       Impact factor: 1.645

6.  The relationship of APOE genotype to neuropsychological performance in long-term cancer survivors treated with standard dose chemotherapy.

Authors:  Tim A Ahles; Andrew J Saykin; Walter W Noll; Charlotte T Furstenberg; Stephen Guerin; Bernard Cole; Leila A Mott
Journal:  Psychooncology       Date:  2003-09       Impact factor: 3.894

7.  Catechol-O-methyltransferase genotype and dopamine regulation in the human brain.

Authors:  Mayada Akil; Bhaskar S Kolachana; Debora A Rothmond; Thomas M Hyde; Daniel R Weinberger; Joel E Kleinman
Journal:  J Neurosci       Date:  2003-03-15       Impact factor: 6.167

8.  Caffeic acid phenethyl ester counteracts doxorubicin-induced chemobrain in Sprague-Dawley rats: Emphasis on the modulation of oxidative stress and neuroinflammation.

Authors:  Marwa A Ali; Esther T Menze; Marianne G Tadros; Mai F Tolba
Journal:  Neuropharmacology       Date:  2020-10-01       Impact factor: 5.250

9.  Longitudinal assessment of cognitive changes associated with adjuvant treatment for breast cancer: impact of age and cognitive reserve.

Authors:  Tim A Ahles; Andrew J Saykin; Brenna C McDonald; Yuelin Li; Charlotte T Furstenberg; Brett S Hanscom; Tamsin J Mulrooney; Gary N Schwartz; Peter A Kaufman
Journal:  J Clin Oncol       Date:  2010-09-13       Impact factor: 44.544

10.  Attenuation of neuroinflammation reverses Adriamycin-induced cognitive impairments.

Authors:  Barrett D Allen; Lauren A Apodaca; Amber R Syage; Mineh Markarian; Al Anoud D Baddour; Harutyun Minasyan; Leila Alikhani; Celine Lu; Brian L West; Erich Giedzinski; Janet E Baulch; Munjal M Acharya
Journal:  Acta Neuropathol Commun       Date:  2019-11-21       Impact factor: 7.801

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  2 in total

1.  Chemobrain: mitoxantrone-induced oxidative stress, apoptotic and autophagic neuronal death in adult CD-1 mice.

Authors:  Ana Dias-Carvalho; Mariana Ferreira; Ana Reis-Mendes; Rita Ferreira; Maria Lourdes Bastos; Eduarda Fernandes; Susana Isabel Sá; João Paulo Capela; Félix Carvalho; Vera Marisa Costa
Journal:  Arch Toxicol       Date:  2022-03-19       Impact factor: 6.168

2.  Grape-Seed-Derived Procyanidin Attenuates Chemotherapy-Induced Cognitive Impairment by Suppressing MMP-9 Activity and Related Blood-Brain-Barrier Damage.

Authors:  Chao Song; Chao Gao; Zhenxin Wang
Journal:  Brain Sci       Date:  2022-04-28
  2 in total

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