Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 0

The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.

Cognitive Impairment Associated with Chemotherapy: Neuroimmunological Interactions, Gut–Brain Axis, and Therapeutic Approaches

Llanes-Cervantes, Beatriz Alejandra, Cruz-Ramos, José Alfonso, Barón-Cárdenas, María Esthela, Zepeda-Olmos, Paola Montserrat, López-Verdín, Sandra, Vargas-López, Jennifer Mariana, de la Mora-Jiménez, Emmanuel·2026·Brain Sciences

Abstract

Chemotherapy is a treatment designed to contain or eradicate neoplastic cells; however, patients may experience various treatment-related adverse effects. Chemotherapy-related cognitive impairment (CRCI), clinically referred to as “chemobrain,” is a frequent complication with a duration ranging from months to years, affecting between 17% and 70% of cancer patients. These cognitive deficits not only impair social, educational, and occupational functioning but may also impact survival outcomes, possibly by interfering with medication adherence and health-related behaviors. Emerging evidence has converged on an integrative cascade in which chemotherapy-induced systemic inflammation, intestinal dysbiosis, blood–brain barrier disruption, microglial/astroglial activation, and impaired hippocampal neurogenesis act in sequence rather than as independent pathways. Underlying pathophysiological mechanisms include neuroinflammation, reduced neurogenesis, loss of dendritic spines, oxidative stress, hormonal changes, epigenetic modifications, and mitochondrial dysfunction. In contrast, repair mechanisms involve complex glial responses, particularly those of astrocytes and microglia. Emerging studies suggest a link between changes in the microbiome and cognitive decline, demonstrating the importance of bidirectional communication in the gut–brain axis. Current research seeks to determine appropriate tests to identify chemobrain. Therefore, several biomarkers, such as GFAP, S100β, and isoprostanes, have been proposed to assess chemobrain, alongside screening tools such as MoCA, MMSE, and CAB-CF, to evaluate cognitive impairment and enable early detection. Pharmacological candidates—including lithium, fluoxetine, methylphenidate, modafinil, metformin, agomelatine, and melatonin—as well as nutritional and lifestyle interventions such as physical exercise, omega-3 fatty acids, curcumin, probiotics, and traditional Chinese medicine formulations—have been investigated, predominantly in animal models. These remain candidate, not validated, therapies; clinical evidence in CRCI populations is limited, heterogeneous, or absent, and well-powered randomized controlled trials are required before any recommendation can be issued. However, optimal strategies for symptom improvement remain unclear, as various approaches have yielded mixed outcomes. This review provides a comprehensive overview of chemobrain, focusing on its molecular mechanisms, interactions with the gut–brain axis, and potential therapeutic targets to improve the quality of life for cancer survivors.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.3390/brainsci16070765

Cites

18 of 18 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 18 references

Research works printed but not linked: 199

  1. Schirrmacher, 2018, From Chemotherapy to Biological Therapy: A Review of Novel Concepts to Reduce the Side Effects of Systemic Cancer Treatment (Review), Int. J. Oncol., 54, 407, 10.3892/ijo.2018.4661 · DOI · Paper page
  2. Mustapha, 2021, Cancer Chemotherapy: A Review Update of the Mechanisms of Actions, Prospects and Associated Problems, BioMed Nat. Appl. Sci., 1, 1
  3. Silberfarb, 1983, Chemotherapy and Cognitive Defects in Cancer Patients, Annu. Rev. Med., 34, 35, 10.1146/annurev.me.34.020183.000343 · DOI
  4. Was, H., Borkowska, A., Bagues, A., Tu, L., Liu, J.Y.H., Lu, Z., Rudd, J.A., Nurgali, K., and Abalo, R. (2022). Mechanisms of Chemotherapy-Induced Neurotoxicity. Front. Pharmacol., 13. · DOI · Paper page
  5. Janelsins, 2014, Prevalence, mechanisms, and management of cancer-related cognitive impairment, Int. Rev. Psychiatry, 26, 102, 10.3109/09540261.2013.864260 · DOI · Paper page
  6. Wefel, 2015, Clinical Characteristics, Pathophysiology, and Management of Noncentral Nervous System Cancer-Related Cognitive Impairment in Adults, CA Cancer J. Clin., 65, 123
  7. Demos-Davies, K., Lawrence, J., and Seelig, D. (2024). Cancer Related Cognitive Impairment: A Downside of Cancer Treatment. Front. Oncol., 14. · DOI
  8. Loef, 2012, Fruit, Vegetables and Prevention of Cognitive Decline or Dementia: A Systematic Review of Cohort Studies, J. Nutr. Health Aging, 16, 626, 10.1007/s12603-012-0097-x · DOI · Paper page
  9. Sherwin, 2012, Estrogen and Cognitive Functioning in Women: Lessons We Have Learned, Behav. Neurosci., 126, 123, 10.1037/a0025539 · DOI · Paper page
  10. Usuki, 1998, Serum Leptin Levels during Cancer Chemotherapy, Ann. Hematol., 77, 191, 10.1007/s002770050441 · doi:10.1007/s002770050441
  11. Rink, 2011, Significance of Brain Tissue Oxygenation and the Arachidonic Acid Cascade in Stroke, Antioxid. Redox Signal, 14, 1889, 10.1089/ars.2010.3474 · DOI · Paper page
  12. Joshi, 2005, Free Radical Mediated Oxidative Stress and Toxic Side Effects in Brain Induced by the Anti Cancer Drug Adriamycin: Insight into Chemobrain, Free Radic. Res., 39, 1147, 10.1080/10715760500143478 · DOI · Paper page
  13. Ren, 2019, Plausible Biochemical Mechanisms of Chemotherapy-Induced Cognitive Impairment (“Chemobrain”), a Condition That Significantly Impairs the Quality of Life of Many Cancer Survivors, Biochim. Biophys. Acta (BBA)-Mol. Basis Dis., 1865, 1088, 10.1016/j.bbadis.2019.02.007 · DOI
  14. Jaiswara, P.K., and Shukla, S.K. (2023). Chemotherapy-Mediated Neuronal Aberration. Pharmaceuticals, 16. · DOI
  15. Ren, 2017, Dysregulation of Cytokine Mediated Chemotherapy Induced Cognitive Impairment, Pharmacol. Res., 117, 267, 10.1016/j.phrs.2017.01.001 · DOI
  16. Ernst, 2014, Neurogenesis in the Striatum of the Adult Human Brain, Cell, 156, 1072, 10.1016/j.cell.2014.01.044 · DOI · Paper page
  17. Ming, 2011, Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions, Neuron, 70, 687, 10.1016/j.neuron.2011.05.001 · DOI · Paper page
  18. Nguyen, 2020, Cellular Mechanisms and Treatments for Chemobrain: Insight from Aging and Neurodegenerative Diseases, EMBO Mol. Med., 12, e12075, 10.15252/emmm.202012075 · DOI · Paper page
  19. Thomas, 2017, Acute Treatment with Doxorubicin Affects Glutamate Neurotransmission in the Mouse Frontal Cortex and Hippocampus, Brain Res., 1672, 10, 10.1016/j.brainres.2017.07.003 · DOI
  20. Wahdan, 2018, Astaxanthin Ameliorates Doxorubicin-Induced Cognitive Impairment (Chemobrain) in Experimental Rat Model: Impact on Oxidative, Inflammatory, and Apoptotic Machineries, Mol. Neurobiol., 55, 5727, 10.1007/s12035-017-0797-7 · DOI · Paper page
  21. Keeney, 2018, Doxorubicin-Induced Elevated Oxidative Stress and Neurochemical Alterations in Brain and Cognitive Decline: Protection by MESNA and Insights into Mechanisms of Chemotherapy-Induced Cognitive Impairment (“chemobrain”), Oncotarget, 9, 30324, 10.18632/oncotarget.25718 · DOI
  22. Kaplan, 2016, Impaired Brain Dopamine and Serotonin Release and Uptake in Wistar Rats Following Treatment with Carboplatin, ACS Chem. Neurosci., 7, 689, 10.1021/acschemneuro.5b00029 · DOI
  23. Dubey, J., Ratnakaran, N., and Koushika, S.P. (2015). Neurodegeneration and Microtubule Dynamics: Death by a Thousand Cuts. Front. Cell. Neurosci., 9. · DOI · Paper page
  24. Pekny, 2016, Reactive Gliosis in the Pathogenesis of CNS Diseases, Biochim. Biophys. Acta (BBA)-Mol. Basis Dis., 1862, 483, 10.1016/j.bbadis.2015.11.014 · DOI · Paper page
  25. Fields, 2014, Glial Biology in Learning and Cognition, Neuroscientist, 20, 426, 10.1177/1073858413504465 · DOI · Paper page
  26. Fardell, 2014, The Impact of Sustained and Intermittent Docetaxel Chemotherapy Regimens on Cognition and Neural Morphology in Healthy Mice, Psychopharmacology, 231, 841, 10.1007/s00213-013-3301-8 · DOI
  27. Christie, 2012, Impaired Cognitive Function and Hippocampal Neurogenesis Following Cancer Chemotherapy, Clin. Cancer Res., 18, 1954, 10.1158/1078-0432.CCR-11-2000 · DOI · Paper page
  28. Carvalho, 2024, Chemotherapy-Induced Cognitive Impairment and Glia: A New Take on Chemobrain?, Toxicol. Appl. Pharmacol., 492, 117085, 10.1016/j.taap.2024.117085 · DOI
  29. Jessen, 2004, Glial Cells, Int. J. Biochem. Cell Biol., 36, 1861, 10.1016/j.biocel.2004.02.023 · DOI · Paper page
  30. Sofroniew, 2010, Astrocytes: Biology and Pathology, Acta Neuropathol., 119, 7, 10.1007/s00401-009-0619-8 · DOI · Paper page
  31. Freeman, 2010, Specification and Morphogenesis of Astrocytes, Science, 330, 774, 10.1126/science.1190928 · DOI · Paper page
  32. Bosetti, 2007, Arachidonic Acid Metabolism in Brain Physiology and Pathology: Lessons from Genetically Altered Mouse Models, J. Neurochem., 102, 577, 10.1111/j.1471-4159.2007.04558.x · DOI
  33. Fan, 2021, A1/A2 Astrocytes in Central Nervous System Injuries and Diseases: Angels or Devils?, Neurochem. Int., 148, 105080, 10.1016/j.neuint.2021.105080 · DOI · Paper page
  34. Wendimu, M.Y., and Hooks, S.B. (2022). Microglia Phenotypes in Aging and Neurodegenerative Diseases. Cells, 11. · DOI · Paper page
  35. Moretti, 2021, Behavioral and Morphological Effects of Resveratrol and Curcumin in Rats Submitted to Doxorubicin-Induced Cognitive Impairment, Res. Vet. Sci., 140, 242, 10.1016/j.rvsc.2021.09.009 · DOI
  36. Liu, 2019, Paclitaxel-Activated Astrocytes Produce Mechanical Allodynia in Mice by Releasing Tumor Necrosis Factor-α and Stromal-Derived Cell Factor 1, J. Neuroinflamm., 16, 209, 10.1186/s12974-019-1619-9 · DOI
  37. Kang, 2018, Chronic Treatment with Combined Chemotherapeutic Agents Affects Hippocampal Micromorphometry and Function in Mice, Independently of Neuroinflammation, Exp. Neurobiol., 27, 419, 10.5607/en.2018.27.5.419 · DOI
  38. Ongnok, 2020, Doxorubicin and Cisplatin Induced Cognitive Impairment: The Possible Mechanisms and Interventions, Exp. Neurol., 324, 113118, 10.1016/j.expneurol.2019.113118 · DOI
  39. Jia, 2023, Inhibition of NLRP3 Alleviated Chemotherapy-Induced Cognitive Impairment in Rats, Neurosci. Lett., 793, 136975, 10.1016/j.neulet.2022.136975 · DOI
  40. Liu, 2023, Resveratrol Improves Paclitaxel-Induced Cognitive Impairment in Mice by Activating SIRT1/PGC-1α Pathway to Regulate Neuronal State and Microglia Cell Polarization, Drug Des. Dev. Ther., 17, 1125, 10.2147/DDDT.S400936 · DOI
  41. Tang, 2022, Paclitaxel Induces Cognitive Impairment via Necroptosis, Decreased Synaptic Plasticity and M1 Polarisation of Microglia, Pharm. Biol., 60, 1556, 10.1080/13880209.2022.2108064 · DOI
  42. Bradfield, 2023, Mild Cognitive Impairment: Diagnosis and Subtypes, Clin. EEG Neurosci., 54, 4, 10.1177/15500594211042708 · DOI
  43. Folstein, 1975, “Mini-Mental State”: A Practical Method for Grading the Cognitive State of Patients for the Clinician, J. Psychiatr. Res., 12, 189, 10.1016/0022-3956(75)90026-6 · DOI · Paper page
  44. Monroe, 2012, Using the Folstein Mini Mental State Exam (MMSE) to Explore Methodological Issues in Cognitive Aging Research, Eur. J. Ageing, 9, 265, 10.1007/s10433-012-0234-8 · DOI
  45. Karimi, L., Mahboub-Ahari, A., Jahangiry, L., Sadeghi-Bazargani, H., and Farahbakhsh, M. (2022). A Systematic Review and Meta-Analysis of Studies on Screening for Mild Cognitive Impairment in Primary Healthcare. BMC Psychiatry, 22. · DOI
  46. Mitchell, 2009, A Meta-Analysis of the Accuracy of the Mini-Mental State Examination in the Detection of Dementia and Mild Cognitive Impairment, J. Psychiatr. Res., 43, 411, 10.1016/j.jpsychires.2008.04.014 · DOI · Paper page
  47. Piccininni, 2023, Should Cognitive Screening Tests Be Corrected for Age and Education? Insights From a Causal Perspective, Am. J. Epidemiol., 192, 93, 10.1093/aje/kwac159 · DOI
  48. Pezzotti, P., Scalmana, S., Mastromattei, A., and Di Lallo, D. (2008). The “Progetto Alzheimer” Working Group The Accuracy of the MMSE in Detecting Cognitive Impairment When Administered by General Practitioners: A Prospective Observational Study. BMC Fam. Pract., 9. · DOI
  49. Mandyla, 2023, Limitations and Recommendations Regarding the Mini-Mental State Examination (MMSE) in Illiterate and Low Educated Older Adults, Psychol. J. Hell. Psychol. Soc., 28, 141, 10.12681/psy_hps.31694 · DOI
  50. Matallana, 2011, The Relationship between Education Level and Mini-Mental State Examination Domains among Older Mexican Americans, J. Geriatr. Psychiatry Neurol., 24, 9, 10.1177/0891988710373597 · DOI
  51. Smailagic, 2015, Mini-Mental State Examination (MMSE) for the Detection of Alzheimer’s Disease and Other Dementias in People with Mild Cognitive Impairment (MCI), Cochrane Database Syst. Rev., 2015, CD010783
  52. Nasreddine, 2005, The Montreal Cognitive Assessment, MoCA: A Brief Screening Tool For Mild Cognitive Impairment, J. Am. Geriatr. Soc., 53, 695, 10.1111/j.1532-5415.2005.53221.x · DOI · Paper page
  53. Shahim, 2013, Cerebrospinal Fluid Biomarkers in Neurological Diseases in Children, Eur. J. Paediatr. Neurol., 17, 7, 10.1016/j.ejpn.2012.09.005 · DOI
  54. Yang, 2015, Glial Fibrillary Acidic Protein: From Intermediate Filament Assembly and Gliosis to Neurobiomarker, Trends Neurosci., 38, 364, 10.1016/j.tins.2015.04.003 · DOI · Paper page
  55. Willemse, 2023, A Multimodal Marker for Cognitive Functioning in Multiple Sclerosis: The Role of NfL, GFAP and Conventional MRI in Predicting Cognitive Functioning in a Prospective Clinical Cohort, J. Neurol., 270, 3851, 10.1007/s00415-023-11676-4 · DOI
  56. Chiang, 2019, Chemotherapy Accelerates Age-Related Development of Tauopathy and Results in Loss of Synaptic Integrity and Cognitive Impairment, Brain Behav. Immun., 79, 319, 10.1016/j.bbi.2019.04.005 · DOI
  57. Bolsewig, 2024, Association of Plasma Amyloid, P-Tau, GFAP, and NfL With CSF, Clinical, and Cognitive Features in Patients With Dementia With Lewy Bodies, Neurology, 102, e209418, 10.1212/WNL.0000000000209418 · DOI
  58. Abbas, 2025, Utility of Plasma GFAP as a Secondary Endpoint for Clinical Trials in Alzheimer’s Disease, J. Prev. Alzheimer’s Dis., 12, 100205, 10.1016/j.tjpad.2025.100205 · DOI
  59. Huynh, 2024, Changes in S100 Calcium-Binding Protein β (S100β) and Cognitive Function from Pre- to Post-Chemotherapy among Women with Breast Cancer, Brain Behav. Immun.-Health, 41, 100860, 10.1016/j.bbih.2024.100860 · DOI
  60. Nehra, 2025, Plasma S100β Is a Predictor for Pathology and Cognitive Decline in Alzheimer’s Disease, Fluids Barriers CNS, 22, 4, 10.1186/s12987-024-00615-8 · DOI
  61. Rokach, 2004, Total Synthesis of Isoprostanes: Discovery and Quantitation in Biological Systems, Chem. Phys. Lipids, 128, 35, 10.1016/j.chemphyslip.2003.09.011 · DOI
  62. Timalsina, 2025, A Review Article on Oxidative Stress Markers F2-Isoprostanes and Presenilin-1 in Alzheimer’s Disease, J. Pharm. Bioallied Sci., 17, S109, 10.4103/jpbs.jpbs_1784_24 · DOI
  63. Hooke, 2021, Biomarkers and Cognitive Function in Children and Adolescents During Maintenance Therapy for Leukemia, Oncol. Nurs. Forum, 48, 623, 10.1188/21.ONF.623-633 · DOI
  64. Ahmad, 2024, Association of Oxidative Stress and Inflammatory Metabolites with Alzheimer’s Disease Cerebrospinal Fluid Biomarkers in Mild Cognitive Impairment, Alzheimer’s Res. Ther., 16, 171, 10.1186/s13195-024-01542-4 · DOI
  65. Alberti, P., Salvalaggio, A., Argyriou, A.A., Bruna, J., Visentin, A., Cavaletti, G., and Briani, C. (2022). Neurological Complications of Conventional and Novel Anticancer Treatments. Cancers, 14. · DOI
  66. Zhao, 2020, Changes in Plasma IL-1β, TNF-α and IL-4 Levels Are Involved in Chemotherapy-Related Cognitive Impairment in Early-Stage Breast Cancer Patients, Am. J. Transl. Res., 12, 3046
  67. Keetile, 2023, Association of Circulating Levels of Inflammatory Cytokines and Chemotherapy-Associated Subjective Cognitive Impairment in a South African Cohort of Breast Cancer Patients, NeuroSci, 4, 296, 10.3390/neurosci4040024 · DOI
  68. Griseta, 2023, Serum Levels of IL-6 Are Associated with Cognitive Impairment in the Salus in Apulia Population-Based Study, Heliyon, 9, e13972, 10.1016/j.heliyon.2023.e13972 · DOI
  69. Garner, 2018, Microglia Priming by Interleukin-6 Signaling Is Enhanced in Aged Mice, J. Neuroimmunol., 324, 90, 10.1016/j.jneuroim.2018.09.002 · DOI
  70. Cheung, Y.T., Lim, S.R., Ho, H.K., and Chan, A. (2013). Cytokines as Mediators of Chemotherapy-Associated Cognitive Changes: Current Evidence, Limitations and Directions for Future Research. PLoS ONE, 8. · DOI
  71. Pascual, 2019, Exosomes as Mediators of Neuron-Glia Communication in Neuroinflammation, Neural Regen. Res., 15, 796, 10.4103/1673-5374.268893 · DOI · Paper page
  72. Koh, Y.Q., Tan, C.J., Toh, Y.L., Sze, S.K., Ho, H.K., Limoli, C.L., and Chan, A. (2020). Role of Exosomes in Cancer-Related Cognitive Impairment. Int. J. Mol. Sci., 21. · DOI
  73. Wang, 2022, Exosomes and Cancer—Diagnostic and Prognostic Biomarkers and Therapeutic Vehicle, Oncogenesis, 11, 54, 10.1038/s41389-022-00431-5 · DOI · Paper page
  74. Chen, E.I., Crew, K.D., Trivedi, M., Awad, D., Maurer, M., Kalinsky, K., Koller, A., Patel, P., Kim Kim, J., and Hershman, D.L. (2015). Identifying Predictors of Taxane-Induced Peripheral Neuropathy Using Mass Spectrometry-Based Proteomics Technology. PLoS ONE, 10. · DOI
  75. Xiang, Y., Xin, J., Le, W., and Yang, Y. (2020). Neurogranin: A Potential Biomarker of Neurological and Mental Diseases. Front. Aging Neurosci., 12. · DOI
  76. DeKosky, 1990, Synapse Loss in Frontal Cortex Biopsies in Alzheimer’s Disease: Correlation with Cognitive Severity, Ann. Neurol., 27, 457, 10.1002/ana.410270502 · DOI · Paper page
  77. Khalil, 2024, Neurofilaments as Biomarkers in Neurological Disorders—Towards Clinical Application, Nat. Rev. Neurol., 20, 269, 10.1038/s41582-024-00955-x · DOI · Paper page
  78. Truffi, 2023, Neurofilament-Light Chain Quantification by Simoa and Ella in Plasma from Patients with Dementia: A Comparative Study, Sci. Rep., 13, 4041, 10.1038/s41598-023-29704-8 · DOI
  79. Velasco, 2024, Plasma Neurofilament Light Chain Levels in Chemotherapy-Induced Peripheral Neurotoxicity According to Type of Anticancer Drug, Eur. J. Neurol., 31, e16369, 10.1111/ene.16369 · DOI
  80. Montassier, 2015, Chemotherapy-Driven Dysbiosis in the Intestinal Microbiome, Aliment. Pharmacol. Ther., 42, 515, 10.1111/apt.13302 · DOI · Paper page
  81. 2018, Microbioma humano, Rev. De La Fac. De Med., 61, 7, 10.22201/fm.24484865e.2018.61.6.02 · doi:10.22201/fm.24484865e.2018.61.6.02
  82. Guarner, 2021, Microbiota Intestinal y Salud, Gastroenterol. Y Hepatol., 44, 519, 10.1016/j.gastrohep.2021.01.009 · DOI
  83. Arboleya, 2012, Facultative to Strict Anaerobes Ratio in the Preterm Infant Microbiota, Gut Microbes, 3, 583, 10.4161/gmic.21942 · DOI · Paper page
  84. Murphy, 2015, The Composition of the Gut Microbiota throughout Life, with an Emphasis on Early Life, Microb. Ecol. Health Dis., 26, 26050
  85. Arumugam, 2011, Enterotypes of the Human Gut Microbiome, Nature, 473, 174, 10.1038/nature09944 · DOI · Paper page
  86. Claesson, 2011, Composition, Variability, and Temporal Stability of the Intestinal Microbiota of the Elderly, Proc. Natl. Acad. Sci. USA, 108, 4586, 10.1073/pnas.1000097107 · DOI · Paper page
  87. Zoetendal, 2008, High-Throughput Diversity and Functionality Analysis of the Gastrointestinal Tract Microbiota, Gut, 57, 1605, 10.1136/gut.2007.133603 · DOI · Paper page
  88. Carabotti, 2015, The Gut-Brain Axis: Interactions between Enteric Microbiota, Central and Enteric Nervous Systems, Ann. Gastroenterol., 28, 203
  89. Bodke, 2022, Role of Probiotics in Human Health, Cureus, 14, e31313
  90. Loh, 2024, Microbiota–Gut–Brain Axis and Its Therapeutic Applications in Neurodegenerative Diseases, Signal Transduct. Target. Ther., 9, 37, 10.1038/s41392-024-01743-1 · DOI · Paper page
  91. Morais, 2021, The Gut Microbiota–Brain Axis in Behaviour and Brain Disorders, Nat. Rev. Microbiol., 19, 241, 10.1038/s41579-020-00460-0 · DOI · Paper page
  92. Bravo, 2011, Ingestion of Lactobacillus Strain Regulates Emotional Behavior and Central GABA Receptor Expression in a Mouse via the Vagus Nerve, Proc. Natl. Acad. Sci. USA, 108, 16050, 10.1073/pnas.1102999108 · DOI · Paper page
  93. Strandwitz, 2019, GABA Modulating Bacteria of the Human Gut Microbiota, Nat. Microbiol., 4, 396, 10.1038/s41564-018-0307-3 · DOI · Paper page
  94. Dalile, 2019, The Role of Short-Chain Fatty Acids in Microbiota–Gut–Brain Communication, Nat. Rev. Gastroenterol. Hepatol., 16, 461, 10.1038/s41575-019-0157-3 · DOI · Paper page
  95. Macfarlane, 2003, Regulation of Short-Chain Fatty Acid Production, Proc. Nutr. Soc., 62, 67, 10.1079/PNS2002207 · DOI · Paper page
  96. Fachi, 2016, Regulation of Immune Cell Function by Short-Chain Fatty Acids, Clin. Transl. Immunol., 5, e73, 10.1038/cti.2016.17 · DOI · Paper page
  97. Vinolo, 2011, Regulation of Inflammation by Short Chain Fatty Acids, Nutrients, 3, 858, 10.3390/nu3100858 · DOI · Paper page
  98. Zhang, R., Ding, N., Feng, X., and Liao, W. (2025). The Gut Microbiome, Immune Modulation, and Cognitive Decline: Insights on the Gut-Brain Axis. Front. Immunol., 16. · DOI
  99. Kasarello, K., Cudnoch-Jedrzejewska, A., and Czarzasta, K. (2023). Communication of Gut Microbiota and Brain via Immune and Neuroendocrine Signaling. Front. Microbiol., 14. · DOI · Paper page
  100. Zhong, 2019, Targeting Strategies for Chemotherapy-Induced Peripheral Neuropathy: Does Gut Microbiota Play a Role?, Crit. Rev. Microbiol., 45, 369, 10.1080/1040841X.2019.1608905 · DOI
  101. Deleemans, J.M., Chleilat, F., Reimer, R.A., Henning, J.-W., Baydoun, M., Piedalue, K.-A., McLennan, A., and Carlson, L.E. (2019). The Chemo-Gut Study: Investigating the Long-Term Effects of Chemotherapy on Gut Microbiota, Metabolic, Immune, Psychological and Cognitive Parameters in Young Adult Cancer Survivors; Study Protocol. BMC Cancer, 19. · DOI
  102. Grant, 2024, Chemotherapy-Induced Gut Microbiome Disruption, Inflammation, and Cognitive Decline in Female Patients with Breast Cancer, Brain Behav. Immun., 120, 208, 10.1016/j.bbi.2024.05.039 · DOI · Paper page
  103. Park, S.-Y., Hwang, B.-O., Lim, M., Ok, S.-H., Lee, S.-K., Chun, K.-S., Park, K.-K., Hu, Y., Chung, W.-Y., and Song, N.-Y. (2021). Oral–Gut Microbiome Axis in Gastrointestinal Disease and Cancer. Cancers, 13. · DOI · Paper page
  104. Boksa, 2025, Oral Microbiome Alterations after Cancer Treatment: A Scoping Review and Analysis, Med. Oncol., 42, 432, 10.1007/s12032-025-02998-6 · DOI
  105. Hong, 2019, Chemotherapy-Induced Oral Mucositis Is Associated with Detrimental Bacterial Dysbiosis, Microbiome, 7, 66, 10.1186/s40168-019-0679-5 · DOI · Paper page
  106. Nodit, 2025, Oral Microbiome and Mycobiome Dynamics in Cancer Therapy-Induced Oral Mucositis, Sci. Data, 12, 463, 10.1038/s41597-025-04671-z · doi:10.1038/s41597-025-04671-z
  107. Zarco, 2012, The Oral Microbiome in Health and Disease and the Potential Impact on Personalized Dental Medicine, Oral Dis., 18, 109, 10.1111/j.1601-0825.2011.01851.x · DOI · Paper page
  108. Kitamoto, 2020, The Intermucosal Connection between the Mouth and Gut in Commensal Pathobiont-Driven Colitis, Cell, 182, 447, 10.1016/j.cell.2020.05.048 · DOI · Paper page
  109. Chaudhry, 2019, Chemotherapy-Induced Cognitive Impairment Is Associated with Increased Inflammation and Oxidative Damage in the Hippocampus, Mol. Neurobiol., 56, 7159, 10.1007/s12035-019-1589-z · DOI
  110. Wardill, 2016, Cytokine-mediated Blood Brain Barrier Disruption as a Conduit for Cancer/Chemotherapy-associated Neurotoxicity and Cognitive Dysfunction, Intl J. Cancer, 139, 2635, 10.1002/ijc.30252 · DOI · Paper page
  111. Alavi, 2026, The Role of the Oral Microbiome in Periodontal Disease: A Systematic Review of Microbial Associations and Therapeutic Implications, Curr. Microbiol., 83, 64, 10.1007/s00284-025-04648-6 · DOI
  112. Singhrao, 2019, Assessing the Role of Porphyromonas Gingivalis in Periodontitis to Determine a Causative Relationship with Alzheimer’s Disease, J. Oral Microbiol., 11, 1563405, 10.1080/20002297.2018.1563405 · DOI
  113. Dominy, 2019, Porphyromonas Gingivalis in Alzheimer’s Disease Brains: Evidence for Disease Causation and Treatment with Small-Molecule Inhibitors, Sci. Adv., 5, eaau3333, 10.1126/sciadv.aau3333 · DOI · Paper page
  114. Li, 2023, GSK3β Rs3107669 Polymorphism Implicates Chemotherapy-Associated Retrospective Memory Deficits in Breast Cancer Survivors, Am. J. Cancer Res., 13, 4961
  115. Li, 2022, COMT Rs737865 Mediates Chemobrain in Breast Cancer Patients with Various Levels of Ki-67, Am. J. Cancer Res., 12, 3185
  116. Li, W., Zhang, Q., Cai, Y., Chen, T., and Cheng, H. (2022). The COMT Genetic Factor Regulates Chemotherapy-Related Prospective Memory Impairment in Survivors With HER2−/+ Breast Cancer. Front. Oncol., 12. · DOI
  117. Patel, 2025, Influence of ApoE Genotype on Doxorubicin-Induced Cognitive Impairment in Juvenile Rats, Sci. Rep., 15, 44620, 10.1038/s41598-025-33104-5 · DOI
  118. Janelsins, 2026, Unraveling the Complexity of Cancer-Related Cognitive Impairment in Breast Cancer—Effect of Differing Treatments and Menopausal Status, JAMA Oncol., 12, 146, 10.1001/jamaoncol.2025.5088 · DOI
  119. Olowofela, 2025, Association of Genetic Predisposition to Inflammation with Cancer-Related Cognitive Impairment and Fatigue in Women Who Received Chemotherapy for Nonmetastatic Breast Cancer, JCO Precis Oncol., 9, e2500303, 10.1200/PO-25-00303 · DOI
  120. Bhatt, K.S., Singh, A., Marwaha, G.S., Ravendranathan, N., Sandhu, I.S., Kim, K., Singh, E., Frisbee, J.C., and Singh, K.K. (2025). Different mechanisms in doxorubicin-induced neurotoxicity: Impact of BRCA mutations. Int. J. Mol. Sci., 26. · DOI
  121. Sheng, 2011, Combined Prostaglandin E1 and Lithium Exert Potent Neuroprotection in a Rat Model of Cerebral Ischemia, Acta Pharmacol. Sin., 32, 303, 10.1038/aps.2010.211 · doi:10.1038/aps.2010.211
  122. Yoneyama, M., Shiba, T., Hasebe, S., Umeda, K., Yamaguchi, T., and Ogita, K. (2014). Lithium Promotes Neuronal Repair and Ameliorates Depression-Like Behavior Following Trimethyltin-Induced Neuronal Loss in the Dentate Gyrus. PLoS ONE, 9. · DOI
  123. Jahandideh, 2023, The Effect of Chronic Lithium Treatment on Hippocampal Progenitor Cells: Transcriptomic Analysis and Systems Pharmacology, Brain Behav., 13, e3215, 10.1002/brb3.3215 · DOI
  124. Nguyen, 2021, Pharmacological Rescue of Cognitive Function in a Mouse Model of Chemobrain, Mol. Neurodegener., 16, 41, 10.1186/s13024-021-00463-2 · DOI
  125. ElBeltagy, 2010, Fluoxetine Improves the Memory Deficits Caused by the Chemotherapy Agent 5-Fluorouracil, Behav. Brain Res., 208, 112, 10.1016/j.bbr.2009.11.017 · DOI
  126. Lyons, L., ELBeltagy, M., Bennett, G., and Wigmore, P. (2012). Fluoxetine Counteracts the Cognitive and Cellular Effects of 5-Fluorouracil in the Rat Hippocampus by a Mechanism of Prevention Rather than Recovery. PLoS ONE, 7. · DOI
  127. Lyons, 2011, Fluoxetine Reverses the Memory Impairment and Reduction in Proliferation and Survival of Hippocampal Cells Caused by Methotrexate Chemotherapy, Psychopharmacology, 215, 105, 10.1007/s00213-010-2122-2 · DOI
  128. Weitzner, 1995, Methylphenidate in the Treatment of Neurobehavioral Slowing Associated with Cancer and Cancer Treatment, J. Neuropsychiatry Clin. Neurosci., 7, 347, 10.1176/jnp.7.3.347 · DOI
  129. Conklin, 2010, Long-Term Efficacy of Methylphenidate in Enhancing Attention Regulation, Social Skills, and Academic Abilities of Childhood Cancer Survivors, J. Clin. Oncol., 28, 4465, 10.1200/JCO.2010.28.4026 · DOI
  130. Miladi, 2019, Psychostimulants for Cancer-Related Cognitive Impairment in Adult Cancer Survivors: A Systematic Review and Meta-Analysis, Support. Care Cancer, 27, 3717
  131. Chiang, 2016, Metformin Activation of AMPK-Dependent Pathways Is Neuroprotective in Human Neural Stem Cells against Amyloid-Beta-Induced Mitochondrial Dysfunction, Exp. Cell Res., 347, 322, 10.1016/j.yexcr.2016.08.013 · DOI
  132. Foretz, 2014, Metformin: From Mechanisms of Action to Therapies, Cell Metab., 20, 953, 10.1016/j.cmet.2014.09.018 · DOI · Paper page
  133. Alhowail, 2021, Research Advances on How Metformin Improves Memory Impairment in “Chemobrain”, Neural Regen. Res., 17, 15, 10.4103/1673-5374.314284 · DOI
  134. 2023, Metformin, Cognitive Function, and Changes in the Gut Microbiome, Endocr. Rev., 45, 210
  135. Tahmi, 2023, Metformin in the Prevention of Alzheimer’s Disease and Alzheimer’s Disease Related Dementias, J. Prev. Alzheimer’s Dis., 10, 706, 10.14283/jpad.2023.113 · DOI
  136. Alhowail, 2019, Ameliorative Effect of Metformin on Cyclophosphamide-Induced Memory Impairment in Mice, Eur. Rev. Med. Pharmacol. Sci., 23, 9660
  137. Alhowail, 2024, Synergistic Effects of Metformin and Fluorouracil on Cognitive Disability via Inducing Neuroinflammation in Rat Models, Int. J. Pharmacol., 20, 1421, 10.3923/ijp.2024.1421.1431 · doi:10.3923/ijp.2024.1421.1431
  138. Chunchai, 2023, Melatonin and Metformin Counteract Cognitive Dysfunction Equally in Male Rats with Doxorubicin-Induced Chemobrain, NeuroToxicology, 94, 158, 10.1016/j.neuro.2022.11.012 · DOI
  139. Alharbi, 2021, DOX and MET Treatment Induces Cognitive Impairment through Downregulation of IL-1-Alpha and IRS-1 in the Rat Brain, Eur. Rev. Med. Pharmacol. Sci., 25, 4106
  140. Usta, Z., Pekgöz, Ş., Şahin, M., Kara, Y., and Özmen, Ö. (2026). Agomelatine Alleviates Methotrexate-Induced Lung Injury by Concurrently Inhibiting CD45/CD68-Positive Immune Cell Infiltration and Modulating the BAX/BCL2 Apoptosis Pathway. J. Appl. Toxicol., jat.70097. · doi:10.1002/jat.70097
  141. Usta, 2026, Agomelatine Restores Apoptotic and Glial Homeostasis in Methotrexate-Induced Cortical Neurotoxicity, J. Pharmacol. Exp. Ther., 393, 104893, 10.1016/j.jpet.2026.104893 · DOI
  142. Caspersen, 1985, Physical Activity, Exercise, and Physical Fitness: Definitions and Distinctions for Health-Related Research, Public Health Rep., 100, 126
  143. Koevoets, 2022, Effect of Physical Exercise on Cognitive Function after Chemotherapy in Patients with Breast Cancer: A Randomized Controlled Trial (PAM Study), Breast Cancer Res., 24, 36, 10.1186/s13058-022-01530-2 · DOI
  144. Lu, 2023, Recent Advances on the Molecular Mechanisms of Exercise-Induced Improvements of Cognitive Dysfunction, Transl. Neurodegener., 12, 9, 10.1186/s40035-023-00341-5 · DOI
  145. Lin, 2006, Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases, Nature, 443, 787, 10.1038/nature05292 · DOI · Paper page
  146. Ye, Y., Lin, H., Wan, M., Qiu, P., Xia, R., He, J., Tao, J., Chen, L., and Zheng, G. (2021). The Effects of Aerobic Exercise on Oxidative Stress in Older Adults: A Systematic Review and Meta-Analysis. Front. Physiol., 12. · DOI
  147. Miranda, M., Morici, J.F., Zanoni, M.B., and Bekinschtein, P. (2019). Brain-Derived Neurotrophic Factor: A Key Molecule for Memory in the Healthy and the Pathological Brain. Front. Cell. Neurosci., 13. · DOI · Paper page
  148. Volosin, 2006, Interaction of Survival and Death Signaling in Basal Forebrain Neurons: Roles of Neurotrophins and Proneurotrophins, J. Neurosci., 26, 7756, 10.1523/JNEUROSCI.1560-06.2006 · DOI · Paper page
  149. McAllister, 1999, Neurotrophins and synaptic plasticity, Annu. Rev. Neurosci., 22, 295, 10.1146/annurev.neuro.22.1.295 · DOI · Paper page
  150. Radahmadi, 2016, Effect of Exercise, Exercise Withdrawal, and Continued Regular Exercise on Excitability and Long-Term Potentiation in the Dentate Gyrus of Hippocampus, Brain Res., 1653, 8, 10.1016/j.brainres.2016.09.045 · DOI
  151. Tsai, 2017, An Acute Bout of Aerobic or Strength Exercise Specifically Modifies Circulating Exerkine Levels and Neurocognitive Functions in Elderly Individuals with Mild Cognitive Impairment, Neuroimage Clin., 17, 272, 10.1016/j.nicl.2017.10.028 · DOI
  152. Vaquero, 2021, Plasticity in Bilateral Hippocampi after a 3-Month Physical Activity Programme in Lung Cancer Patients, Eur. J. Neurol., 28, 1324, 10.1111/ene.14670 · DOI
  153. Ren, 2022, Effects of Physical Exercise on Cognitive Function of Breast Cancer Survivors Receiving Chemotherapy: A Systematic Review of Randomized Controlled Trials, Breast, 63, 113, 10.1016/j.breast.2022.03.014 · DOI
  154. Park, 2018, Physical Exercise Prevents Cognitive Impairment by Enhancing Hippocampal Neuroplasticity and Mitochondrial Function in Doxorubicin-Induced Chemobrain, Neuropharmacology, 133, 451, 10.1016/j.neuropharm.2018.02.013 · DOI
  155. Crupi, 2013, N-3 Fatty Acids: Role in Neurogenesis and Neuroplasticity, Curr. Med. Chem., 20, 2953, 10.2174/09298673113209990140 · DOI · Paper page
  156. Horrocks, 1999, Health Benefits of Docosahexaenoic Acid (DHA), Pharmacol. Res., 40, 211, 10.1006/phrs.1999.0495 · DOI · Paper page
  157. James, 2010, Fish Oil and Rheumatoid Arthritis: Past, Present and Future, Proc. Nutr. Soc., 69, 316, 10.1017/S0029665110001564 · DOI
  158. Heshmati, 2019, Omega-3 Fatty Acids Supplementation and Oxidative Stress Parameters: A Systematic Review and Meta-Analysis of Clinical Trials, Pharmacol. Res., 149, 104462, 10.1016/j.phrs.2019.104462 · DOI · Paper page
  159. Orchard, 2017, Clearing the Fog: A Review of the Effects of Dietary Omega-3 Fatty Acids and Added Sugars on Chemotherapy-Induced Cognitive Deficits, Breast Cancer Res. Treat., 161, 391, 10.1007/s10549-016-4073-8 · DOI
  160. Yee, 2010, Ω-3 Fatty Acid Supplements in Women at High Risk of Breast Cancer Have Dose-Dependent Effects on Breast Adipose Tissue Fatty Acid Composition123, Am. J. Clin. Nutr., 91, 1185, 10.3945/ajcn.2009.29036 · DOI
  161. Ghoreishi, Z., Esfahani, A., Djazayeri, A., Djalali, M., Golestan, B., Ayromlou, H., Hashemzade, S., Asghari Jafarabadi, M., Montazeri, V., and Keshavarz, S.A. (2012). Omega-3 Fatty Acids Are Protective against Paclitaxel-Induced Peripheral Neuropathy: A Randomized Double-Blind Placebo Controlled Trial. BMC Cancer, 12. · DOI · Paper page
  162. Langius, 2012, Oral Nutritional Supplements Containing N-3 Polyunsaturated Fatty Acids Affect Quality of Life and Functional Status in Lung Cancer Patients during Multimodality Treatment: An RCT, Eur. J. Clin. Nutr., 66, 399, 10.1038/ejcn.2011.214 · DOI · Paper page
  163. Wu, Y.-Q., Dang, R.-L., Tang, M.-M., Cai, H.-L., Li, H.-D., Liao, D.-H., He, X., Cao, L.-J., Xue, Y., and Jiang, P. (2016). Long Chain Omega-3 Polyunsaturated Fatty Acid Supplementation Alleviates Doxorubicin-Induced Depressive-Like Behaviors and Neurotoxicity in Rats: Involvement of Oxidative Stress and Neuroinflammation. Nutrients, 8. · DOI
  164. Ma, T., Liaset, B., Hao, Q., Petersen, R.K., Fjære, E., Ngo, H.T., Lillefosse, H.H., Ringholm, S., Sonne, S.B., and Treebak, J.T. (2011). Sucrose Counteracts the Anti-Inflammatory Effect of Fish Oil in Adipose Tissue and Increases Obesity Development in Mice. PLoS ONE, 6. · DOI
  165. Hauser, 2018, Effects of Omega-3 Fatty Acids and Sugar on Attention in the Spontaneously Hypertensive Rat, J. Funct. Foods, 48, 676, 10.1016/j.jff.2018.07.057 · DOI
  166. Hewlings, S.J., and Kalman, D.S. (2017). Curcumin: A Review of Its’ Effects on Human Health. Foods, 6. · DOI · Paper page
  167. Gupta, 2012, Therapeutic Roles of Curcumin: Lessons Learned from Clinical Trials, AAPS J., 15, 195, 10.1208/s12248-012-9432-8 · DOI · Paper page
  168. Panahi, 2016, Effects of Curcumin on Serum Cytokine Concentrations in Subjects with Metabolic Syndrome: A Post-Hoc Analysis of a Randomized Controlled Trial, Biomed. Pharmacother., 82, 578, 10.1016/j.biopha.2016.05.037 · DOI · Paper page
  169. Zhou, 2011, Targets of Curcumin, Curr. Drug Targets, 12, 332, 10.2174/138945011794815356 · DOI · Paper page
  170. Kunnumakkara, 2018, Chronic Diseases, Inflammation, and Spices: How Are They Linked?, J. Transl. Med., 16, 14, 10.1186/s12967-018-1381-2 · DOI · Paper page
  171. Anand, 2007, Bioavailability of Curcumin: Problems and Promises, Mol. Pharm., 4, 807, 10.1021/mp700113r · DOI · Paper page
  172. Hegde, 2023, Curcumin Formulations for Better Bioavailability: What We Learned from Clinical Trials Thus Far?, ACS Omega, 8, 10713, 10.1021/acsomega.2c07326 · DOI · Paper page
  173. Aggarwal, 2003, Anticancer Potential of Curcumin: Preclinical and Clinical Studies, Anticancer Res., 23, 363
  174. Abdelsalam, 2025, Empagliflozin Dampens Doxorubicin-Induced Chemobrain in Rats: The Possible Involvement of Oxidative Stress and PI3K/Akt/mTOR/NF-κB/TNF-α Signaling Pathways, Mol. Neurobiol., 62, 3480, 10.1007/s12035-024-04499-5 · DOI
  175. Sharma, 2004, Phase I Clinical Trial of Oral Curcumin: Biomarkers of Systemic Activity and Compliance, Clin. Cancer Res., 10, 6847, 10.1158/1078-0432.CCR-04-0744 · DOI · Paper page
  176. Panahi, 2014, Adjuvant Therapy with Bioavailability-Boosted Curcuminoids Suppresses Systemic Inflammation and Improves Quality of Life in Patients with Solid Tumors: A Randomized Double-Blind Placebo-Controlled Trial, Phytother. Res., 28, 1461, 10.1002/ptr.5149 · DOI · Paper page
  177. Mahendra, 2024, Improving Cognitive Function with Intermittent Dose Escalation of Curcumin Extract in Chemotherapy-Induced Cognitive Impairment Patients: A Randomized Controlled Trial, Adv. Tradit. Med., 24, 813, 10.1007/s13596-023-00737-8 · DOI
  178. Weber, 2007, Curcumin Downregulates NF-kB and Related Genes in Patients with Multiple Myeloma: Results of a Phase I/II Study, Blood, 110, 1177, 10.1182/blood.V110.11.1177.1177 · doi:10.1182/blood.v110.11.1177.1177
  179. Chang, 2023, The Bioavailability, Metabolism and Microbial Modulation of Curcumin-Loaded Nanodelivery Systems, Adv. Colloid Interface Sci., 318, 102933, 10.1016/j.cis.2023.102933 · DOI
  180. Sabet, 2021, Recent Advances to Improve Curcumin Oral Bioavailability, Trends Food Sci. Technol., 110, 253, 10.1016/j.tifs.2021.02.006 · DOI · Paper page
  181. Boroughani, 2024, Nanocurcumin in Cancer Treatment: A Comprehensive Systematic Review, Discov. Oncol., 15, 515, 10.1007/s12672-024-01272-x · doi:10.1007/s12672-024-01272-x
  182. Yuan, 2026, Yifei Sanjie Pill Combined with Gefitinib Reduces the Progression of EGFR-TKIs-Resistant Non-Small Cell Lung Cancer via YAP/ANKRD1 Axis, Phytomedicine, 155, 158003, 10.1016/j.phymed.2026.158003 · DOI
  183. Wu, 2026, Elucidating the Mechanism of Traditional Chinese Medicine Formula (Yifei-Sanjie Pill) in Alleviating the Chemobrain Based on Network Pharmacology and Experimental Verification, J. Tradit. Complement. Med., 16, 17, 10.1016/j.jtcme.2024.11.008 · doi:10.1016/j.jtcme.2024.11.008
  184. Juan, 2022, Probiotic Supplement Attenuates Chemotherapy-Related Cognitive Impairment in Patients with Breast Cancer: A Randomised, Double-Blind, and Placebo-Controlled Trial, Eur. J. Cancer, 161, 10, 10.1016/j.ejca.2021.11.006 · DOI · Paper page
  185. Hill, 2014, The International Scientific Association for Probiotics and Prebiotics Consensus Statement on the Scope and Appropriate Use of the Term Probiotic, Nat. Rev. Gastroenterol. Hepatol., 11, 506, 10.1038/nrgastro.2014.66 · DOI
  186. Khorashadizadeh, 2024, The Role of Microbiome and Probiotics in Chemo-Radiotherapy-Induced Diarrhea: A Narrative Review of the Current Evidence, Cancer Rep., 7, e70029
  187. Lin, 2023, Neuroprotective Effects of Probiotic Lactobacillus Reuteri GMNL-263 in the Hippocampus of Streptozotocin-Induced Diabetic Rats, Probiotics Antimicrob. Proteins, 15, 1287, 10.1007/s12602-022-09982-w · DOI
  188. Luck, 2020, Bifidobacteria Shape Host Neural Circuits during Postnatal Development by Promoting Synapse Formation and Microglial Function, Sci. Rep., 10, 7737, 10.1038/s41598-020-64173-3 · DOI
  189. Kim, 2020, Probiotic Supplementation Improves Cognitive Function and Mood with Changes in Gut Microbiota in Community-Dwelling Older Adults: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial, J. Gerontol. Ser. A Biol. Sci. Med. Sci., 76, 32, 10.1093/gerona/glaa090 · DOI · Paper page
  190. Lee, 2014, Effects of 12 Weeks of Probiotic Supplementation on Quality of Life in Colorectal Cancer Survivors: A Double-Blind, Randomized, Placebo-Controlled Trial, Dig. Liver Dis., 46, 1126, 10.1016/j.dld.2014.09.004 · DOI
  191. Liu, 2023, Probiotic Supplements Are Effective in People with Cognitive Impairment: A Meta-Analysis of Randomized Controlled Trials, Nutr. Rev., 81, 1091, 10.1093/nutrit/nuac113 · DOI
  192. Chen, 2025, The Impact of Probiotics Therapy on Cognitive and Metabolic Characteristics in Patients with Cognitive Impairment: An Umbrella Review of Meta-Analysis of Randomized Controlled Trials, Eur. J. Pharmacol., 994, 177326, 10.1016/j.ejphar.2025.177326 · DOI
  193. Bayraktar, 2022, Melatonin Is Effective in Attenuating Cisplatin-induced Neurotoxicity, J. Biochem. Mol. Tox, 36, e23075, 10.1002/jbt.23075 · DOI
  194. Waseem, 2016, Neuroprotective Effects of Melatonin as Evidenced by Abrogation of Oxaliplatin Induced Behavioral Alterations, Mitochondrial Dysfunction and Neurotoxicity in Rat Brain, Mitochondrion, 30, 168, 10.1016/j.mito.2016.08.001 · DOI
  195. Suwannakot, K., Sritawan, N., Prajit, R., Aranarochana, A., Sirichoat, A., Pannangrong, W., Wigmore, P., and Welbat, J.U. (2021). Melatonin Protects against the Side-Effects of 5-Fluorouracil on Hippocampal Neurogenesis and Ameliorates Antioxidant Activity in an Adult Rat Hippocampus and Prefrontal Cortex. Antioxidants, 10. · DOI
  196. Briones, T.L., and Woods, J. (2011). Chemotherapy-Induced Cognitive Impairment Is Associated with Decreases in Cell Proliferation and Histone Modifications. BMC Neurosci., 12. · DOI
  197. Wang, 2015, Chemobrain: A Critical Review and Causal Hypothesis of Link between Cytokines and Epigenetic Reprogramming Associated with Chemotherapy, Cytokine, 72, 86, 10.1016/j.cyto.2014.12.006 · DOI · Paper page
  198. Khilar, S., Dembinska-Kenner, A., Hall, H., Syrmos, N., Ligarotti, G.K.I., Plaha, P., Apostolopoulos, V., Chibbaro, S., Barbagallo, G.M.V., and Ganau, M. (2025). Towards a New Dawn for Neuro-Oncology: Nanomedicine at the Service of Drug Delivery for Primary and Secondary Brain Tumours. Brain Sci., 15. · DOI
  199. Boykoff, 2009, Confronting Chemobrain: An in-Depth Look at Survivors’ Reports of Impact on Work, Social Networks, and Health Care Response, J. Cancer Surviv., 3, 223, 10.1007/s11764-009-0098-x · DOI · Paper page

Metadata

Authors
Llanes-Cervantes, B. A., Cruz-Ramos, J. A., Barón-Cárdenas, M. E., Zepeda-Olmos, P. M., López-Verdín, S., Vargas-López, J. M., & de la Mora-Jiménez, E.
Venue
Brain Sciences
Publisher
MDPI AG
Published
2026-07-21
Volume
16
Issue
7
Pages
765
ISSN
2076-3425
Cited by
0
References
18
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Cognitive Impairment Associated with Chemotherapy: Neuroimmunological Interactions, Gut–Brain Axis, and Therapeutic Approaches. https://app.cochat.ai/papers/10.3390/brainsci16070765
The paper
Llanes-Cervantes, B. A., Cruz-Ramos, J. A., Barón-Cárdenas, M. E., Zepeda-Olmos, P. M., López-Verdín, S., Vargas-López, J. M., & de la Mora-Jiménez, E. (2026). Cognitive Impairment Associated with Chemotherapy: Neuroimmunological Interactions, Gut–Brain Axis, and Therapeutic Approaches. Brain Sciences. https://doi.org/10.3390/brainsci16070765

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.