The Role of Heat Shock Proteins in Oxidative Stress Oksidatif Streste Isı Şoku Proteinlerinin Rolü
Keywords:
Cell İnjury, heat shock proteins, oxidative stress, reactive oxygen speciesAbstract
Oxidative stress is at the forefront of these changes that develop during inflammation, which is at the core of diseases. Oxidative stress occurs due to both the excessive release of oxidation products as a result of metabolic activity and a deficiency in the antioxidant system. Oxidative stress, which has recently become a focus of scientific interest, plays a role in the pathogenesis of many diseases. While increased oxidative stress triggers inflammation, a reduction in oxidative stress contributes to the healing process of the disease. Therefore, oxidative stress is beneficial both in understanding diseases and in monitoring various treatment processes. Various biomarkers are used to monitor oxidative stress during inflammation. Heat shock proteins, whose use is gaining momentum in current research, are protein groups that are released during cell injury due to increased intracellular oxidation-induced temperature. Heat shock proteins are responsible for cell development, cycle, metabolism, signaling, proliferation, apoptosis, differentiation, and, in particular, the proper folding of proteins. These proteins are also called stress proteins because they increase under various stress conditions that cause inflammation, such as infection, dehydration, toxicity, starvation, and physical and chemical factors. Heat shock proteins are classified into different groups based on their function and molecular structure. In this research, the structure, types, functions and possible contributions of heat shock proteins to scientific studies were discussed.
References
Adwas, A. A., Elsayed, A., Azab, A. E., & Quwaydir, F. A. (2019). Oxidative stress and antioxidant mechanisms in human body. J. Appl. Biotechnol. Bioeng, 6(1), 43-47. Beere, H. M., & Green, D. R. (2001). Stress management–heat shock protein-70 and the regulation of apoptosis. Trends in cell biology, 11(1), 6-10.
Berestoviy, V. O., Mahmood, A., Venckivska, I. B., Ginzburg, V. G., Sokol, I. V., Berestoviy, O. O., & Govsieiev, D. O. (2021). The overview and role of heat shock proteins (HSP) especially HSP 60 and 70 in reproduction and other pathologies (a literature review). Медичні перспективи, 26(1), 54-62.
Concannon, C. G., Gorman, A. M., & Samali, A. (2003). On the role of HSP27 in regulating apoptosis. Apoptosis, 8, 61-70. Çenesiz, S. (2020). The role of oxidant and antioxidant parameters in the infectious diseases: A systematic literature review. Kafkas Universitesi Veteriner Fakultesi Dergisi, 26(6).
Demirci-Çekiç, S., Özkan, G., Avan, A. N., Uzunboy, S., Çapanoğlu, E., & Apak, R. (2022). Biomarkers of oxidative stress and antioxidant defense. Journal of pharmaceutical and biomedical analysis, 209, 114477. Dong, J., Guo, L., Liao, Z., Zhang, M., Zhang, M., Wang, T., ... & Wen, F. (2013). Increased expression of heat shock protein 70 in chronic obstructive pulmonary disease. International immunopharmacology, 17(3), 885-893. Dörtbudak, M. B., Demircioğlu, M., & Kapucuk, F. S. (2025). Micromeria congesta Alleviates LPSInduced Inflammation, Apoptosis, Oxidative Stress and DNA Damage in Rat Heart and Kidneys. Veterinary Medicine and Science, 11(2), e70264.
Dörtbudak, M. B., Demircioğlu, M., Demircioğlu, İ., Nicotra, M., & Di Cerbo, A. (2025). Pathological Investigation of the Effect of Bovine Colostrum Against 5-FU-Induced Liver, Kidney, and Heart Toxicity in Rats. Life, 15(4), 564. 23
Dörtbudak, M. B., Şeker, U., Demircioğlu, M., & Demircioğlu, I. (2025). Effect of Gundelia tournefortii extract on diabetic gastropathy: involvement of inflammation, apoptosis, oxidative stress, and histopathology. Veterinary Research Forum, 16(3): 133-139.
Frijhoff, J., Winyard, P. G., Zarkovic, N., Davies, S. S., Stocker, R., Cheng, D., ... & Ghezzi, P. (2015). Clinical relevance of biomarkers of oxidative stress. Antioxidants & redox signaling, 23(14), 1144-1170.
Caparrós, P., De Filippis, L., Gul, A., Hasanuzzaman, M., Ozturk, M., Altay, V., & Lao, M. T. (2021). Oxidative stress and antioxidant metabolism under adverse environmental conditions: a review. The Botanical Review, 87, 421-466.
Garrido, C., Brunet, M., Didelot, C., Zermati, Y., Schmitt, E., & Kroemer, G. (2006). Heat shock proteins 27 and 70: anti-apoptotic proteins with tumorigenic properties. Cell cycle, 5(22), 2592- 2601. Garrido, C., Schmitt, E., Candé, C., Vahsen, N., Parcellier, A., & Kroemer, G. (2003). HSP27 and HSP70: potentially oncogenic apoptosis inhibitors. Cell cycle, 2(6), 578-583.
Giaginis, C., Daskalopoulou, S. S., Vgenopoulou, S., Sfiniadakis, I., Kouraklis, G., & Theocharis, S. E. (2009). Heat Shock Protein-27,-60 and-90 expression in gastric cancer: association with clinicopathological variables and patient survival. BMC gastroenterology, 9, 1-10.
Glaessgen, A., Jonmarker, S., Lindberg, A., Nilsson, B. O., Lewensohn, R., Ekman, P., ... & Egevad, L. (2008). Heat shock proteins 27, 60 and 70 as prognostic markers of prostate cancer. Apmis, 116(10), 888-895.
Grundtman, C., Kreutmayer, S. B., Almanzar, G., Wick, M. C., & Wick, G. (2011). Heat shock protein 60 and immune inflammatory responses in atherosclerosis. Arteriosclerosis, thrombosis, and vascular biology, 31(5), 960-968.
Habich, C., & Burkart, V. (2007). Heat shock protein 60: regulatory role on innate immune cells. Cellular and Molecular Life Sciences, 64, 742-751.
Hamelin, C., Cornut, E., Poirier, F., Pons, S., Beaulieu, C., Charrier, J. P., ... & Choquet‐Kastylevsky, G. (2011). Identification and verification of heat shock protein 60 as a potential serum marker for colorectal cancer. The FEBS journal, 278(24), 4845-4859.
Hassan, F. U., Nawaz, A., Rehman, M. S., Ali, M. A., Dilshad, S. M., & Yang, C. (2019). Prospects of HSP70 as a genetic marker for thermo-tolerance and immuno-modulation in animals under climate change scenario. Animal Nutrition, 5(4), 340-350.
Hrudka, J., Jelinkova, K., Fišerová, H., Matěj, R., Mandys, V., & Waldauf, P. (2021). Heat shock proteins 27, 70, and 110: expression and prognostic significance in colorectal cancer. Cancers, 13(17), 4407.
Hu, C., Yang, J., Qi, Z., Wu, H., Wang, B., Zou, F., ... & Liu, Q. (2022). Heat shock proteins: Biological functions, pathological roles, and therapeutic opportunities. MedComm, 3(3), e161.
Indharty, S., Japardi, I., Tandean, S., Siahaan, A. M., Loe, M. L., & Riawan, W. (2020). Efficacy of Neuroprotection from Curcumin through Heat Shock Protein 70 Induction in Traumatic Brain Injury–Rat Model. Open Access Macedonian Journal of Medical Sciences, 8(A), 593-596. Jakubczyk, K., Dec, K., Kałduńska, J., Kawczuga, D., Kochman, J., & Janda, K. (2020). Reactive oxygen species-sources, functions, oxidative damage. Polski Merkuriusz Lekarski: Organ Polskiego Towarzystwa Lekarskiego, 48(284), 124-127.
Jee, H. (2016). Size dependent classification of heat shock proteins: a mini-review. Journal of exercise rehabilitation, 12(4), 255.
Jomova, K., Raptova, R., Alomar, S. Y., Alwasel, S. H., Nepovimova, E., Kuca, K., & Valko, M. (2023). Reactive oxygen species, toxicity, oxidative stress, and antioxidants: Chronic diseases and aging. Archives of toxicology, 97(10), 2499-2574.
Karapınar, Z., İlhan, F., Dinçer, E., & Yıldırım, S. (2017). Pathology and phylogenetic analysis of capripoxvirus in naturally infected sheep sheeppox virus.
Kiang, J. G., & Tsokos, G. C. (1998). Heat shock protein 70 kDa: molecular biology, biochemistry, and physiology. Pharmacology & therapeutics, 80(2), 183-201.
Li, J., & Buchner, J. (2013). Structure, function and regulation of the HSP90 machinery. Biomedical journal, 36(3). Lushchak, V. I., & Lushchak, O. (2021). Interplay between reactive oxygen and nitrogen species in living organisms. Chemico-Biological Interactions, 349, 109680.
Ma, X., Deng, D., & Chen, W. (2017). Inhibitors and Activators of SOD, GSH-Px, and CAT. Enzyme inhibitors and activators, 29, 207-224.
Malik, J. A., & Lone, R. (2021). Heat shock proteins with an emphasis on HSP 60. Molecular Biology Reports, 48(10), 6959-6969.
Mayer, M. P., & Bukau, B. (2005). HSP70 chaperones: cellular functions and molecular mechanism. Cellular and molecular life sciences, 62, 670-684.
Moussa, Z., Judeh, Z. M., & Ahmed, S. A. (2019). Nonenzymatic exogenous and endogenous antioxidants. Free radical medicine and biology, 1, 11-22.
Oyagbemi, A. A., Omobowale, T. O., Ola‐Davies, O. E., Asenuga, E. R., Ajibade, T. O., Adejumobi, O. A., ... & Yakubu, M. A. (2018). Quercetin attenuates hypertension induced by sodium fluoride via reduction in oxidative stress and modulation of HSP 70/ERK/PPARγ signaling pathways. Biofactors, 44(5), 465-479.
Öztürk, E., Kahveci, N., Özlük, K., & Yılmazlar, T. (2009). Isı şok proteinleri. Turkish Journal of Surgery/Ulusal Cerrahi Dergisi, 25(4).
Öztürk, E., Kaymak, E., Akin, A., Karabulut, D., & Yakan, B. (2023). Thymoquinone attenuates doxorubicin-induced lung damage via heat shock proteins, inflammation and endoplasmic reticulum stress. Journal of the Hellenic Veterinary Medical Society, 74(2), 5569-5576.
Park, C. J., & Seo, Y. S. (2015). Heat shock proteins: a review of the molecular chaperones for plant immunity. The plant pathology journal, 31(4), 323.
Pearl, L. H., & Prodromou, C. (2006). Structure and mechanism of the HSP90 molecular chaperone machinery. Annu. Rev. Biochem., 75(1), 271-294.
Pires, E. S., & Khole, V. V. (2009). A block in the road to fertility: autoantibodies to heat-shock protein 90-β in human ovarian autoimmunity. Fertility and sterility, 92(4), 1395-1409.
Pisoschi, A. M., & Pop, A. (2015). The role of antioxidants in the chemistry of oxidative stress: A review. European journal of medicinal chemistry, 97, 55-74. Prodromou, C. (2016). Mechanisms of HSP90 regulation. Biochemical Journal, 473(16), 2439-2452.
Pulur, A., Karaca, İ., & Yıldırım Karaca, S. (2017). Isı şok protein 70 (Heat Shock Proteın 70) düzeylerinin normal ve preeklamptik gebelerdeki seviyesi. Tepecik Eğit. ve Araşt. Hast. Dergisi 2017; 27(2):88-92
Puppel, K., Kapusta, A., & Kuczyńska, B. (2015). The etiology of oxidative stress in the various species of animals, a review. Journal of the Science of Food and Agriculture, 95(11), 2179-2184.
Qu, B., Jia, Y., Liu, Y., Wang, H., Ren, G., & Wang, H. (2015). The detection and role of heat shock protein 70 in various nondisease conditions and disease conditions: a literature review. Cell Stress and Chaperones, 20(6), 885-892.
Sies, H., Berndt, C., & Jones, D. P. (2017). Oxidative stress. Annual review of biochemistry, 86(1), 715-748.
Sönmez, M. F., Ozdemir, Ş., Guzel, M., & Kaymak, E. M. İ. N. (2017). The ameliorative effects of vinpocetine on apoptosis and HSP-70 expression in testicular torsion in rats. Biotechnic & Histochemistry, 92(2), 92-99. 27
Sreedhar, A. S., Kalmár, É., Csermely, P., & Shen, Y. F. (2004). HSP90 isoforms: functions, expression and clinical importance. FEBS letters, 562(1-3), 11-15.
Tkáčová, J., & Angelovičová, M. (2012). Heat shock proteins (HSPs): a review. Scientific Papers Animal Science and Biotechnologies, 45(1), 349-349.
Tremosini, S., Forner, A., Boix, L., Vilana, R., Bianchi, L., Reig, M., ... & Bruix, J. (2012). Prospective validation of an immunohistochemical panel (glypican 3, heat shock protein 70 and glutamine synthetase) in liver biopsies for diagnosis of very early hepatocellular carcinoma. Gut, 61(10), 1481-1487. Uztimür, M., Ünal, C. N., Dörtbudak, M. B., Fırat, R., & Ekinci, A. İ. (2025). Assessment of brain injury in cattle with Theileria annulata: Neuron-specific biomarkers, inflammation, oxidative stress and apoptosis. The Veterinary Journal, 309, 106269.
Vidyasagar, A., Wilson, N. A., & Djamali, A. (2012). Heat shock protein 27 (HSP27): biomarker of disease and therapeutic target. Fibrogenesis & tissue repair, 5, 1-7.
Wandinger, S. K., Richter, K., & Buchner, J. (2008). The HSP90 chaperone machinery. Journal of Biological Chemistry, 283(27), 18473-18477. Wang, X., Chen, M., Zhou, J., & Zhang, X. (2014). HSP27, 70 and 90, anti-apoptotic proteins, in clinical cancer therapy. International journal of oncology, 45(1), 18-30.
Wilhelmus, M. M. M., Otte‐Höller, I., Wesseling, P., De Waal, R. M. W., Boelens, W. C., & Verbeek, M. M. (2006). Specific association of small heat shock proteins with the pathological hallmarks of Alzheimer's disease brains. Neuropathology and applied neurobiology, 32(2), 119-130.
Yusuf, F., Adewiah, S., & Fatchiyah, F. (2018). The level short chain fatty acids and HSP 70 in colorectal cancer and non-colorectal cancer. Acta Informatica Medica, 26(3), 160.
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