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A Preliminary Study on the Relationship between Serum Heparan Sulfate and Cancer-Related Cognitive Impairment: The Moderating Role of Oxidative Stress in Patients with Colorectal Cancer

Wang, Danhui, Wang, Teng, Zhu, Min, Sun, Jun, Zhou, Zhou, Chen, Jinghua, Teng, Liping·2022·Current Oncology

Abstract

Cancer-related cognitive impairment (CRCI) has been frequently reported in colorectal cancer survivors. Heparan sulfate (HS) was gradually considered to be related to cognitive disorders. The effect and potential mechanism of HS on CRCI in colorectal cancer patients were unexplored. In this study, all participants were divided into a cognitive impaired group and a cognitive normal group. The concentrations of oxidative stress factors and HS in serum were detected. Associations among HS, oxidative stress factors and CRCI were evaluated. Participants with cognitive impairment exhibited increased levels of HS, GSH, SOD and MDA, compared to the patients with normal cognitive performance. The independent significant association was found between HS and CRCI after controlling for various covariates. The higher concentrations of HS were related to the decreased cognitive performance among survivors who reported higher levels of GSH (β = 0.080, p = 0.002). Moreover, the nonlinear association between the level of HS and cognitive scores was confirmed using the restricted cubic splines (p < 0.001). These results indicated that the increased concentrations of circulating HS had a nonlinear negative connection with cognitive performance in colorectal cancer survivors, which was moderated by GSH. HS might be a new biomolecule for the identification and management of patients with CRCI.

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Research works printed but not linked: 46

  1. Lange, 2019, Cancer-related cognitive impairment: An update on state of the art, detection, and management strategies in cancer survivors, Ann. Oncol., 30, 1925, 10.1093/annonc/mdz410 · DOI · Paper page
  2. Underwood, 2019, Cognitive effects of adjuvant endocrine therapy in older women treated for early-stage breast cancer: A 1-year longitudinal study, Support. Care Cancer., 27, 3035, 10.1007/s00520-018-4603-5 · DOI
  3. Janelsins, 2018, Longitudinal Trajectory and Characterization of Cancer-Related Cognitive Impairment in a Nationwide Cohort Study, J. Clin. Oncol., 36, 3231, 10.1200/JCO.2018.78.6624 · DOI · Paper page
  4. Vardy, 2014, Cognitive function and fatigue after diagnosis of colorectal cancer, Ann. Oncol., 25, 2404, 10.1093/annonc/mdu448 · DOI
  5. 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. Mol. Basis. Dis., 1865, 1088, 10.1016/j.bbadis.2019.02.007 · DOI
  6. 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
  7. 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
  8. Williams, 2018, Associations between inflammatory markers and cognitive function in breast cancer patients receiving chemotherapy, J. Neuroimmunol., 314, 17, 10.1016/j.jneuroim.2017.10.005 · DOI
  9. Ganz, 2013, Does tumor necrosis factor-alpha (TNF-α) play a role in post-chemotherapy cerebral dysfunction?, Brain Behav. Immun., 30, S99, 10.1016/j.bbi.2012.07.015 · DOI
  10. Mulloy, 2017, Mast cell glycosaminoglycans, Glycoconj. J., 34, 351, 10.1007/s10719-016-9749-0 · DOI
  11. Szatmári, T., Mundt, F., Kumar-Singh, A., Möbus, L., Ötvös, R., Hjerpe, A., and Dobra, K. (2017). Molecular targets and signaling pathways regulated by nuclear translocation of syndecan-1. BMC Cell Biol., 18. · DOI
  12. Stewart, 2014, Heparan sulfate in the nucleus and its control of cellular functions, Matrix. Biol., 35, 56, 10.1016/j.matbio.2013.10.009 · DOI
  13. Gulberti, 2020, The role of heparan sulfate maturation in cancer: A focus on the 3O-sulfation and the enigmatic 3O-sulfotransferases (HS3STs), Semin. Cancer Biol., 62, 68, 10.1016/j.semcancer.2019.10.009 · DOI
  14. Puangmalai, 2020, Internalization mechanisms of brain-derived tau oligomers from patients with Alzheimer’s disease, progressive supranuclear palsy and dementia with Lewy bodies, Cell Death Dis., 11, 314, 10.1038/s41419-020-2503-3 · DOI
  15. Ordiales, 2020, Heparan Sulfate Proteoglycans Undergo Differential Expression Alterations in Alzheimer Disease Brains, J. Neuropathol. Exp. Neurol., 79, 474, 10.1093/jnen/nlaa016 · DOI
  16. Alcalde, 2021, Alterations in the Expression of the Genes Responsible for the Synthesis of Heparan Sulfate in Brains With Alzheimer Disease, J. Neuropathol. Exp. Neurol., 80, 446, 10.1093/jnen/nlab028 · DOI
  17. Hippensteel, 2019, Circulating heparan sulfate fragments mediate septic cognitive dysfunction, J. Clin. Investig., 129, 1779, 10.1172/JCI124485 · DOI
  18. Reynolds, 2016, Heparan sulfate proteoglycans mediate Aβ-induced oxidative stress and hypercontractility in cultured vascular smooth muscle cells, Mol. Neurodegener., 11, 9, 10.1186/s13024-016-0073-8 · DOI
  19. Bigger, 2018, Anatomical changes and pathophysiology of the brain in mucopolysaccharidosis disorders, Mol. Genet. Metab., 125, 322, 10.1016/j.ymgme.2018.08.003 · DOI
  20. Jacobs, 2007, Evaluation of the functional assessment of cancer therapy cognitive scale with hematopoietic stem cell transplant patients, J. Pain Symptom Manag., 33, 13, 10.1016/j.jpainsymman.2006.06.011 · DOI
  21. Joly, 2012, French version of the Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) version 3, Support. Care Cancer, 20, 3297, 10.1007/s00520-012-1439-2 · DOI
  22. Cheung, 2013, Psychometric properties and measurement equivalence of the English and Chinese versions of the functional assessment of cancer therapy-cognitive in Asian patients with breast cancer, Value Health, 16, 1001, 10.1016/j.jval.2013.06.017 · DOI
  23. Cheung, 2014, Minimal clinically important difference (MCID) for the functional assessment of cancer therapy: Cognitive function (FACT-Cog) in breast cancer patients, J. Clin. Epidemiol., 67, 811, 10.1016/j.jclinepi.2013.12.011 · DOI
  24. Ruan, 2020, Demographically Corrected Normative Z Scores on the Neuropsychological Test Battery in Cognitively Normal Older Chinese Adults, Dement Geriatr Cogn Disord., 49, 375, 10.1159/000505618 · DOI
  25. Wong, 2018, Neuropsychological Criteria for Mild Cognitive Impairment in the Framingham Heart Study’s Old-Old, Dement. Geriatr. Cogn. Disord., 46, 253, 10.1159/000493541 · DOI
  26. Ihle, 2019, Cognitive Reserve Mediates the Relation between Openness to Experience and Smaller Decline in Executive Functioning, Dement. Geriatr. Cogn. Disord., 48, 39, 10.1159/000501822 · DOI
  27. Duff, 2016, Demographically corrected normative data for the Hopkins Verbal Learning Test-Revised and Brief Visuospatial Memory Test-Revised in an elderly sample, Appl. Neuropsychol. Adult., 23, 179, 10.1080/23279095.2015.1030019 · doi:10.1080/23279095.2015.1030019
  28. Morimoto, 2021, Clearance of heparan sulfate in the brain prevents neurodegeneration and neurocognitive impairment in MPS II mice, Mol. Ther., 29, 1853, 10.1016/j.ymthe.2021.01.027 · DOI
  29. Vardy, 2015, Cognitive Function in Patients With Colorectal Cancer Who Do and Do Not Receive Chemotherapy: A Prospective, Longitudinal, Controlled Study, J. Clin. Oncol., 33, 4085, 10.1200/JCO.2015.63.0905 · DOI · Paper page
  30. Dhillon, 2018, Perceived cognitive impairment in people with colorectal cancer who do and do not receive chemotherapy, J. Cancer Surviv., 12, 178, 10.1007/s11764-017-0656-6 · DOI · Paper page
  31. Vivek, 2022, Cross sectional association between cytomegalovirus seropositivity, inflammation and cognitive impairment in elderly cancer survivors, Cancer Causes Control, 33, 81, 10.1007/s10552-021-01504-3 · DOI
  32. Chen, 2018, Gray matter density reduction associated with adjuvant chemotherapy in older women with breast cancer, Breast Cancer Res. Treat., 172, 363, 10.1007/s10549-018-4911-y · DOI
  33. Wouters, 2016, Neurocognitive function of lymphoma patients after treatment with chemotherapy, Acta Oncol., 55, 1121, 10.1080/0284186X.2016.1189092 · DOI
  34. Mounier, N.M., Abdel-Maged, A.E., Wahdan, S.A., Gad, A.M., and Azab, S.S. (2020). Chemotherapy-induced cognitive impairment (CICI): An overview of etiology and pathogenesis. Life Sci., 258. · DOI
  35. Paterson, 2021, Association of renal impairment with cognitive dysfunction in the Northern Ireland Cohort for the Longitudinal Study of Ageing (NICOLA), Nephrol. Dial. Transplant., 36, 1492, 10.1093/ndt/gfab182 · DOI
  36. Stephan, 2019, Subjective Age and Cystatin C Among Older Adults, J. Gerontol. B. Psychol. Sci. Soc. Sci., 74, 382, 10.1093/geronb/gbx124 · DOI
  37. Wang, 2021, Nutrition Impact Symptom Clusters in Patients With Head and Neck Cancer Receiving Concurrent Chemoradiotherapy, J. Pain Symptom Manage., 62, 277, 10.1016/j.jpainsymman.2020.12.013 · doi:10.1016/j.jpainsymman.2020.12.013
  38. Cardoso, C.V., de Barros, M.P., Bachi, A.L.L., Bernardi, M.M., Kirsten, T.B., de Fátima Monteiro Martins, M., Rocha, P.R.D., da Silva Rodrigues, P., and Bondan, E.F. (2020). Chemobrain in rats: Behavioral, morphological, oxidative and inflammatory effects of doxorubicin administration. Behav. Brain. Res., 378. · DOI
  39. Sun, 2019, Superoxide dismutase activity and risk of cognitive decline in older adults: Findings from the Chinese Longitudinal Healthy Longevity Survey, Exp. Gerontol., 118, 72, 10.1016/j.exger.2019.01.010 · DOI
  40. Lang, 2020, Elevated activity of plasma superoxide dismutase in never-treated first-episode schizophrenia patients: Associated with depressive symptoms, Schizophr. Res., 222, 291, 10.1016/j.schres.2020.05.032 · DOI
  41. Sugawara, 2002, Overexpression of copper/zinc superoxide dismutase in transgenic rats protects vulnerable neurons against ischemic damage by blocking the mitochondrial pathway of caspase activation, J. Neurosci., 22, 209, 10.1523/JNEUROSCI.22-01-00209.2002 · DOI · Paper page
  42. Gibson, 2020, Treating cancer therapy-related cognitive impairment, Nat. Med., 26, 1174, 10.1038/s41591-020-1014-1 · DOI
  43. Zhang, 2021, Heparanase overexpression impedes perivascular clearance of amyloid-β from murine brain: Relevance to Alzheimer’s disease, Acta. Neuropathol. Commun., 9, 84, 10.1186/s40478-021-01182-x · DOI
  44. Devinsky, 2013, Glia and epilepsy: Excitability and inflammation, Trends Neurosci., 36, 174, 10.1016/j.tins.2012.11.008 · DOI · Paper page
  45. Okuyama, 2019, Iduronate-2-Sulfatase with Anti-human Transferrin Receptor Antibody for Neuropathic Mucopolysaccharidosis II: A Phase 1/2 Trial, Mol. Ther., 27, 456, 10.1016/j.ymthe.2018.12.005 · DOI
  46. Zhang, 2021, Collagen/heparan sulfate porous scaffolds loaded with neural stem cells improve neurological function in a rat model of traumatic brain injury, Neural. Regen. Res., 16, 1068, 10.4103/1673-5374.300458 · doi:10.4103/1673-5374.300458

Metadata

Authors
Wang, D., Wang, T., Zhu, M., Sun, J., Zhou, Z., Chen, J., & Teng, L.
Venue
Current Oncology
Publisher
MDPI AG
Published
2022-04-12
Volume
29
Issue
4
Pages
2681-2694
ISSN
1718-7729
Cited by
3
References
6
Language
en
Funders
  • National Natural Science Foundation of China (82172583)
  • Top Talent Support Program for young and middle-aged people of Wuxi Health Committee (BJ 2020041)

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CoChat. (2026). Citation check: A Preliminary Study on the Relationship between Serum Heparan Sulfate and Cancer-Related Cognitive Impairment: The Moderating Role of Oxidative Stress in Patients with Colorectal Cancer. https://app.cochat.ai/papers/10.3390/curroncol29040219
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Wang, D., Wang, T., Zhu, M., Sun, J., Zhou, Z., Chen, J., & Teng, L. (2022). A Preliminary Study on the Relationship between Serum Heparan Sulfate and Cancer-Related Cognitive Impairment: The Moderating Role of Oxidative Stress in Patients with Colorectal Cancer. Current Oncology. https://doi.org/10.3390/curroncol29040219

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