Ahmadi A, Sheikholeslami-Vatani D, Ghaeeni S, Baazm M. The effects of different training modalities on monocarboxylate transporters MCT1 and MCT4, hypoxia inducible factor-1α (HIF-1α), and PGC-1α gene expression in rat skeletal muscles. Mol Biol Rep. 2021 Mar;48(3):2153-2161. doi:
https://doi.org/10.1007/s11033-021-06224-0
Ahmadi Hekmatikar, A. (2023). Correspondence: work smart or work hard in patients with metastatic breast cancer: emphasizing the importance of immunological and lactate changes. Supportive Care in Cancer, 32(1), 59. doi:
https://doi.org/10.1007/s00520-023-08284-3
Ahmadi Hekmatikar, A., Haghshenas, R., & Mohammad Sadeghipor, A. (2019). The effect of carbohydrate supplementation and pure water on interleukin 10, glucose and hematological indexes in male football players. Sport Physiology & Management Investigations, 11(4), 135-145. doi:
https://www.sportrc.ir/article_105715.html
Ahmadi Hekmatikar, A., Nelson, A., & Petersen, A. (2023). Highlighting the idea of exerkines in the management of cancer patients with cachexia: novel insights and a critical review. BMC Cancer, 23(1), 889. doi:
https://doi.org/10.1186/s12885-023-11391-3
Apostolova, P., & Pearce, E. L. (2022). Lactic acid and lactate: revisiting the physiological roles in the tumor microenvironment. Trends in immunology, 43(12), 969–977. doi:
https://doi.org/10.1016/j.it.2022.10.005
Brizel, D. M., Schroeder, T., Scher, R. L., Walenta, S., Clough, R. W., Dewhirst, M. W., & Mueller-Klieser, W. (2001). Elevated tumor lactate concentrations predict for an increased risk of metastases in head-and-neck cancer. International journal of radiation oncology, biology, physics, 51(2), 349–353. doi:
https://doi.org/10.1016/s0360-3016(01)01630-3
Brooks G. A. (1986). The lactate shuttle during exercise and recovery. Medicine and science in sports and exercise, 18(3), 360–368. doi:
https://doi.org/10.1249/00005768-198606000-00019
Brooks G. A. (2018). The Science and Translation of Lactate Shuttle Theory. Cell metabolism, 27(4), 757–785. doi:
https://doi.org/10.1016/j.cmet.2018.03.008
Brooks, G. A., Osmond, A. D., Arevalo, J. A., Curl, C. C., Duong, J. J., Horning, M. A., Moreno Santillan, D. D., & Leija, R. G. (2022). Lactate as a major myokine and exerkine. Nature Reviews Endocrinology, 18(11), 712-712. doi:
https://doi.org/10.1038/s41574-022-00724-0
Ceci, C., García-Chico, C., Atzori, M. G., Lacal, P. M., Lista, S., Santos-Lozano, A., Graziani, G., & Pinto-Fraga, J. (2024). Impact of Physical Exercise on Melanoma Hallmarks: Current Status of Preclinical and Clinical Research. Journal of Cancer, 15(1), 1–19. doi:
https://doi.org/10.7150/jca.88559
Certo, M., Llibre, A., Lee, W., & Mauro, C. (2022). Understanding lactate sensing and signalling. Trends in endocrinology and metabolism: TEM, 33(10), 722–735. doi:
https://doi.org/10.1016/j.tem.2022.07.004
Clemente-Suárez, V. J., Martín-Rodríguez, A., Redondo-Flórez, L., Ruisoto, P., Navarro-Jiménez, E., Ramos-Campo, D. J., & Tornero-Aguilera, J. F. (2023). Metabolic Health, Mitochondrial Fitness, Physical Activity, and Cancer. Cancers, 15(3), 814. doi:
https://doi.org/10.3390/cancers15030814
Coles, L., Litt, J., Hatta, H., & Bonen, A. (2004). Exercise rapidly increases expression of the monocarboxylate transporters MCT1 and MCT4 in rat muscle. The Journal of physiology, 561(Pt 1), 253–261. doi:
https://doi.org/10.1113/jphysiol.2004.073478
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019). Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches. Front Oncol, 9, 1143. doi:
https://doi.org/10.3389/fonc.2019.01143
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019). Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches. Frontiers in oncology, 9, 1143. doi:
https://doi.org/10.3389/fonc.2019.01143
de la Cruz-López, K. G., Castro-Muñoz, L. J., Reyes-Hernández, D. O., García-Carrancá, A., & Manzo-Merino, J. (2019). Lactate in the Regulation of Tumor Microenvironment and Therapeutic Approaches [Review]. Front Oncol, 9. doi:
https://doi.org/10.3389/fonc.2019.01143
Ding, J., Karp, J. E., & Emadi, A. (2017). Elevated lactate dehydrogenase (LDH) can be a marker of immune suppression in cancer: Interplay between hematologic and solid neoplastic clones and their microenvironments. Cancer biomarkers: section A of Disease markers, 19(4), 353–363. doi:
https://doi.org/10.3233/CBM-160336
Domínguez, R., Maté-Muñoz, J. L., Serra-Paya, N., & Garnacho-Castaño, M. V. (2018). Lactate Threshold as a Measure of Aerobic Metabolism in Resistance Exercise. International journal of sports medicine, 39(3), 163–172. doi:
https://doi.org/10.1055/s-0043-122740
Dunn, G. P., Bruce, A. T., Ikeda, H., Old, L. J., & Schreiber, R. D. (2002). Cancer immunoediting: from immunosurveillance to tumor escape. Nature immunology, 3(11), 991–998. doi:
https://doi.org/10.1038/ni1102-991
Gentil, P., Oliveira, E., & Bottaro, M. (2006). Time under tension and blood lactate response during four different resistance training methods. Journal of physiological anthropology, 25(5), 339-344.
Gladden, L. B. (2004). Lactate metabolism: a new paradigm for the third millennium. J Physiol, 558(Pt 1), 5-30. doi:
https://doi.org/10.1113/jphysiol.2003.058701
Harjes, U. (2017). More lactate, please. Nature Reviews Cancer, 17(12), 707-707. doi:
https://doi.org/10.1038/nrc.2017.101
Hubbard J. L. (1973). The effect of exercise on lactate metabolism. The Journal of physiology, 231(1), 1–18. doi:
https://doi.org/10.1113/jphysiol.1973.sp010216
Hunt, T. K., Aslam, R., Hussain, Z., & Beckert, S. (2008). Lactate, with oxygen, incites angiogenesis. Advances in experimental medicine and biology, 614, 73–80. doi:
https://doi.org/10.1007/978-0-387-74911-2_9.
Ishihara, S., Hata, K., Hirose, K., Okui, T., Toyosawa, S., Uzawa, N., Nishimura, R., & Yoneda, T. (2022). The lactate sensor GPR81 regulates glycolysis and tumor growth of breast cancer. Scientific Reports, 12(1), 6261. doi:
https://doi.org/10.1038/s41598-022-10143-w
Juel, C., Klarskov, C., Nielsen, J. J., Krustrup, P., Mohr, M., & Bangsbo, J. (2004). Effect of high-intensity intermittent training on lactate and H+ release from human skeletal muscle. American journal of physiology. Endocrinology and metabolism, 286(2), E245–E251. doi:
https://doi.org/10.1152/ajpendo.00303.2003.
Koelwyn, G. J., Zhuang, X., Tammela, T., Schietinger, A., & Jones, L. W. (2020). Exercise and immunometabolic regulation in cancer. Nature Metabolism, 2(9), 849-857. doi:
https://doi.org/10.1038/s42255-020-00277-4
Kon, M., Ebi, Y., & Nakagaki, K. (2022). Hormonal, metabolic, and angiogenic responses to all-out sprint interval exercise under systemic hyperoxia. Growth Hormone & IGF Research, 63, 101445.
Kroemer, G., Chan, T. A., Eggermont, A. M., & Galluzzi, L. (2024). Immunosurveillance in clinical cancer management. CA: a cancer journal for clinicians, 74(2), 187-202. doi:
https://doi.org/10.3322/caac.21818
Lavín-Pérez, A. M., Collado-Mateo, D., Abbasi, S., Ferreira-Júnior, J. B., & Hekmatikar, A. H. A. (2023). Effects of exercise on immune cells with tumor-specific activity in breast cancer patients and survivors: a systematic review and meta-analysis. Supportive Care in Cancer, 31(9), 507. doi:
https://doi.org/10.1007/s00520-023-07968-0
Li, X., Yang, Y., Zhang, B., Lin, X., Fu, X., An, Y., Zou, Y., Wang, J.-X., Wang, Z., & Yu, T. (2022). Lactate metabolism in human health and disease. Signal Transduction and Targeted Therapy, 7(1), 1-22. doi:
https://doi.org/10.1038/s41392-022-01151-3
Liu, S., Zhao, H., Hu, Y., Yan, C., Mi, Y., Li, X., Tao, D., & Qin, J. (2022). Lactate promotes metastasis of normoxic colorectal cancer stem cells through PGC-1α-mediated oxidative phosphorylation. Cell Death & Disease, 13(7), 651. doi:
https://doi.org/10.1038/s41419-022-05111-1
Martins-Costa, H. C., Diniz, R. C. R., Lima, F. V., Machado, S. C., Almeida, R. S. V. d., Andrade, A. G. P. d., & Chagas, M. H. (2016). Longer repetition duration increases muscle activation and blood lactate response in matched resistance training protocols. Motriz: Revista de Educação Física, 22, 35-41. doi:
https://doi.org/10.1590/S1980-65742016000100005
McTiernan, A. (2008). Mechanisms linking physical activity with cancer. Nature Reviews Cancer, 8(3), 205-211. doi:
https://doi.org/10.1038/nrc2325
Mok, J., Brown, M.-J., Akam, E. C., & Morris, M. A. (2022). The lasting effects of resistance and endurance exercise interventions on breast cancer patient mental wellbeing and physical fitness. Scientific Reports, 12(1), 3504. doi:
https://doi.org/10.1038/s41598-022-07446-3
Morland, C., Andersson, K. A., Haugen, Ø. P., Hadzic, A., Kleppa, L., Gille, A., Rinholm, J. E., Palibrk, V., Diget, E. H., & Kennedy, L. H. (2017). Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1. Nature communications, 8(1), 1-9. doi:
https://doi.org/10.1038/ncomms15557
Otonkoski, T., Jiao, H., Kaminen-Ahola, N., Tapia-Paez, I., Ullah, M. S., Parton, L. E., Schuit, F., Quintens, R., Sipilä, I., & Mayatepek, E. (2007). Physical exercise–induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic β cells. The American Journal of Human Genetics, 81(3), 467-474. doi:
https://doi.org/10.1086/520960
Pennington, Z., Goodwin, M. L., Westbroek, E. M., Cottrill, E., Ahmed, A. K., & Sciubba, D. M. (2019). Lactate and cancer: spinal metastases and potential therapeutic targets (part 2). Ann Transl Med, 7(10). doi:
https://doi.org/10.21037/atm.2019.01.85
Pennington, Z., Goodwin, M. L., Westbroek, E. M., Cottrill, E., Ahmed, A. K., & Sciubba, D. M. (2019). Lactate and cancer: spinal metastases and potential therapeutic targets (part 2). Ann Transl Med, 7(10), 221. doi:
https://doi.org/10.21037/atm.2019.01.85
Pérez-Tomás, R., & Pérez-Guillén, I. (2020). Lactate in the tumor microenvironment: an essential molecule in cancer progression and treatment. Cancers, 12(11), 3244. doi:
https://doi.org/10.3390/cancers12113244
Rahmani, A., Gorzi, A., & Ajali Rad, Z. (2021). The Effect of Endurance Training, Detraining and Shock Training on Monocarboxylate Transporters in the Gastrocnemius Muscle and Endurance Performance of Male Rats. Journal of Sport Biosciences, 12(4), 437-452. doi:
https://doi.org/10.22059/jsb.2020.303284.1402
Rami, M., Rahdar, S., Ahmadi Hekmatikar, A., & Awang Daud, D. M. (2023). Highlighting the novel effects of high-intensity interval training on some histopathological and molecular indices in the heart of type 2 diabetic rats. Frontiers in Endocrinology, 14, 1175585. doi:
https://doi.org/10.3389/fendo.2023.1175585
Rizwan, A., Serganova, I., Khanin, R., Karabeber, H., Ni, X., Thakur, S., Zakian, K. L., Blasberg, R., & Koutcher, J. A. (2013). Relationships between LDH-A, lactate, and metastases in 4T1 breast tumors. Clinical Cancer Research, 19(18), 5158-5169.
San-Millán, I., & Brooks, G. A. (2017). Reexamining cancer metabolism: lactate production for carcinogenesis could be the purpose and explanation of the Warburg Effect. Carcinogenesis, 38(2), 119-133. doi:
https://doi.org/10.1093/carcin/bgw127
SEVERSON, R. K., NOMURA, A. M., GROVE, J. S., & STEMMERMANN, G. N. (1989). A prospective analysis of physical activity and cancer. American Journal of Epidemiology, 130(3), 522-529. doi:
https://doi.org/10.1093/oxfordjournals.aje.a115366
Sharma, D., Singh, M., Gupta, R., Kumar, V., Kumar, V., & Rani, R. (2022). Intervention on lactate in cancer: A promising approach for the development of cancer therapeutics. Advances in Cancer Biology - Metastasis, 5, 100058. doi:
https://doi.org/https://doi.org/10.1016/j.adcanc.2022.100058
Smith-Turchyn, J., & Mukherjee, S. D. (2024). Factors influencing the decision of individuals with breast cancer to join an exercise oncology trial. Journal of Cancer Education, 1-9. doi:
https://doi.org/10.1007/s13187-024-02403-2
Sonveaux, P., Végran, F., Schroeder, T., Wergin, M. C., Verrax, J., Rabbani, Z. N., De Saedeleer, C. J., Kennedy, K. M., Diepart, C., & Jordan, B. F. (2008). Targeting lactate-fueled respiration selectively kills hypoxic tumor cells in mice. The Journal of clinical investigation, 118(12), 3930-3942. URL:
https://www.jci.org/articles/view/36843
Stallknecht, B., Vissing, J., & Galbo, H. (1998). Lactate production and clearance in exercise. Effects of training. A mini‐review. Scandinavian journal of medicine & science in sports, 8(3), 127-131. doi:
https://doi.org/10.1111/j.1600-0838.1998.tb00181.x
Suzuki, K., Hekmatikar, A. H. A., Jalalian, S., Abbasi, S., Ahmadi, E., Kazemi, A., Ruhee, R. T., & Khoramipour, K. (2022). The Potential of Exerkines in Women’s COVID-19: A New Idea for a Better and More Accurate Understanding of the Mechanisms behind Physical Exercise. International journal of environmental research and public health, 19(23), 15645. doi:
https://doi.org/10.3390/ijerph192315645
Takimoto, M., Takeyama, M., & Hamada, T. (2013). Possible involvement of AMPK in acute exercise-induced expression of monocarboxylate transporters MCT1 and MCT4 mRNA in fast-twitch skeletal muscle. Metabolism, 62(11), 1633-1640. doi:
https://doi.org/10.1016/j.metabol.2013.06.010
Tayebi, S. M., Hekmatikar, A. A., Ghanbari-Niaki, A., & Fathi, R. (2020). Ghrelin behavior in exercise and training. J Med. Sci, 27, 85-111.
Tomlin, D. L., & Wenger, H. A. (2001). The relationship between aerobic fitness and recovery from high intensity intermittent exercise. Sports Medicine, 31(1), 1-11. doi:
https://doi.org/10.2165/00007256-200131010-00001
Wang, Q., & Zhou, W. (2021). Roles and molecular mechanisms of physical exercise in cancer prevention and treatment. Journal of Sport and Health Science, 10(2), 201-210. doi:
https://doi.org/10.1016/j.jshs.2020.07.008
Weltman, A., Stamford, B. A., Moffatt, R. J., & Katch, V. L. (1977). Exercise recovery, lactate removal, and subsequent high intensity exercise performance. Research Quarterly. American Alliance for Health, Physical Education and Recreation, 48(4), 786-796. doi:
https://doi.org/10.1080/10671315.1977.10615493
Westerlind, K. C. (2003). Physical activity and cancer prevention—mechanisms. Medicine & Science in Sports & Exercise, 35(11), 1834-1840.