Acknowledgement
This research was funded by the Bisa Research Grant of Keimyung University in 2023 (Project No: 20230327).
References
- Basak, D., Arrighi, S., Darwiche, Y. and Deb, S. (2021) Comparison of anticancer drug toxicities: paradigm shift in adverse effect profile. Life (Basel) 12, 48. https://doi.org/10.3390/life12010048
- Bedard, K. and Krause, K. H. (2007) The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol. Rev. 87, 245-313. https://doi.org/10.1152/physrev.00044.2005
- Bulavin, D. V. and Fornace, A. J., Jr. (2004) p38 MAP kinase's emerging role as a tumor suppressor. Adv. Cancer Res. 92, 95-118. https://doi.org/10.1016/S0065-230X(04)92005-2
- Chen, H. Y., Huang, T. C., Shieh, T. M., Wu, C. H., Lin, L. C. and Hsia, S. M. (2017) Isoliquiritigenin induces autophagy and inhibits ovarian cancer cell growth. Int. J. Mol. Sci. 18, 2025-2039. https://doi.org/10.3390/ijms18102025
- Choi, Y., Park, S., Lee, S., Shin, H. E., Kwon, S., Choi, J. K., Lee, M. H., Seo, S. Y. and Lee, Y. (2023) Cremastranone-derived homoisoflavanes suppress the growth of breast cancer cells via cell cycle arrest and caspase-independent cell death. Biomol. Ther. (Seoul) 31, 526-535. https://doi.org/10.4062/biomolther.2023.057
- Choudhari, A. S., Mandave, P. C., Deshpande, M., Ranjekar, P. and Prakash, O. (2019) Phytochemicals in cancer treatment: from preclinical studies to clinical practice. Front. Pharmacol. 10, 1614.
- Chun, K. S. and Joo, S. H. (2022) Modulation of reactive oxygen species to overcome 5-fluorouracil resistance. Biomol. Ther. (Seoul) 30, 479-489. https://doi.org/10.4062/biomolther.2022.017
- Conciatori, F., Ciuffreda, L., Bazzichetto, C., Falcone, I., Pilotto, S., Bria, E., Cognetti, F. and Milella, M. (2018) mTOR cross-talk in cancer and potential for combination therapy. Cancers 10, 23-52. https://doi.org/10.3390/cancers10010023
- Coulthard, L. R., White, D. E., Jones, D. L., McDermott, M. F. and Burchill, S. A. (2009) p38(MAPK): stress responses from molecular mechanisms to therapeutics. Trends Mol. Med. 15, 369-379. https://doi.org/10.1016/j.molmed.2009.06.005
- Franklin, C., Livingstone, E., Roesch, A., Schilling, B. and Schadendorf, D. (2017) Immunotherapy in melanoma: recent advances and future directions. Eur. J. Surg. Oncol. 43, 604-611. https://doi.org/10.1016/j.ejso.2016.07.145
- Hernández, G., Lal, H., Fidalgo, M., Guerrero, A., Zalvide, J., Force, T. and Pombo, C. M. (2011) A novel cardioprotective p38-MAPK/mTOR pathway. Exp. Cell Res. 317, 2938-2949. https://doi.org/10.1016/j.yexcr.2011.09.011
- Hirchaud, F., Hermetet, F., Ablise, M., Fauconnet, S., Vuitton, D. A., Prétet, J. L. and Mougin, C. (2013) Isoliquiritigenin induces caspase-dependent apoptosis via downregulation of HPV16 E6 expression in cervical cancer Ca Ski cells. Planta Med. 79, 1628-1635. https://doi.org/10.1055/s-0033-1350956
- Hsu, Y. L., Kuo, P. L. and Lin, C. C. (2005) Isoliquiritigenin induces apoptosis and cell cycle arrest through p53-dependent pathway in Hep G2 cells. Life Sci. 77, 279-292. https://doi.org/10.1016/j.lfs.2004.09.047
- Huynh, J., Chand, A., Gough, D. and Ernst, M. (2019) Therapeutically exploiting STAT3 activity in cancer - using tissue repair as a road map. Nat. Rev. Cancer 19, 82-96. https://doi.org/10.1038/s41568-018-0090-8
- Hwang, S. Y., Wi, K., Yoon, G., Lee, C. J., Lee, S. I., Jung, J. G., Jeong, H. W., Kim, J. S., Choi, C. H., Na, C. S., Shim, J. H. and Lee, M. H. (2023) Licochalcone D inhibits skin epidermal cells transformation through the regulation of AKT signaling pathways. Biomol. Ther. (Seoul) 31, 682-691. https://doi.org/10.4062/biomolther.2023.162
- Jiang, H., Zuo, J., Li, B., Chen, R., Luo, K., Xiang, X., Lu, S., Huang, C., Liu, L., Tang, J. and Gao, F. (2023) Drug-induced oxidative stress in cancer treatments: angel or devil? Redox Biol. 63, 102754. https://doi.org/10.1016/j.redox.2023.102754
- Jung, J. I., Lim, S. S., Choi, H. J., Cho, H. J., Shin, H. K., Kim, E. J., Chung, W. Y., Park, K. K. and Park, J. H. (2006) Isoliquiritigenin induces apoptosis by depolarizing mitochondrial membranes in prostate cancer cells. J. Nutr. Biochem. 17, 689-696. https://doi.org/10.1016/j.jnutbio.2005.11.006
- Kim, D. H., Park, J. E., Chae, I. G., Park, G., Lee, S. and Chun, K. S. (2017) Isoliquiritigenin inhibits the proliferation of human renal carcinoma Caki cells through the ROS-mediated regulation of the Jak2/STAT3 pathway. Oncol. Rep. 38, 575-583. https://doi.org/10.3892/or.2017.5677
- Kim, N., Kwon, J., Shin, U. S. and Jung, J. (2023) Stimulatory anticancer effect of resveratrol mediated by G protein-coupled estrogen receptor in colorectal cancer. Biomol. Ther. (Seoul) 31, 655-660. https://doi.org/10.4062/biomolther.2023.072
- Lee, S. O., Joo, S. H., Kwak, A. W., Lee, M. H., Seo, J. H., Cho, S. S., Yoon, G., Chae, J. I. and Shim, J. H. (2021) Podophyllotoxin induces ROS-mediated apoptosis and cell cycle arrest in human colorectal cancer cells via p38 MAPK signaling. Biomol. Ther. (Seoul) 29, 658-666. https://doi.org/10.4062/biomolther.2021.143
- Li, M., Lu, G., Ma, X., Wang, R., Chen, X., Yu, Y. and Jiang, C. (2022) Anti-inflammation of isoliquiritigenin via the inhibition of NF-κB and MAPK in LPS-stimulated MAC-T cells. BMC Vet. Res. 18, 320.
- Li, Y., Zhao, H., Wang, Y., Zheng, H., Yu, W., Chai, H., Zhang, J., Falck, J. R., Guo, A. M., Yue, J., Peng, R. and Yang, J. (2013) Isoliquiritigenin induces growth inhibition and apoptosis through downregulating arachidonic acid metabolic network and the deactivation of PI3K/Akt in human breast cancer. Toxicol. Appl. Pharmacol. 272, 37-48. https://doi.org/10.1016/j.taap.2013.05.031
- Liu, Y. X., Wang, J., Guo, J., Wu, J., Lieberman, H. B. and Yin, Y. (2008) DUSP1 is controlled by p53 during the cellular response to oxidative stress. Mol. Cancer Res. 6, 624-633. https://doi.org/10.1158/1541-7786.MCR-07-2019
- Luo, F., Tang, Y., Zheng, L., Yang, Y., Gao, H., Tian, S., Chen, H., Tang, C., Tang, S., Man, Q. and Wu, Y. (2023) Isoliquiritigenin inhibits the growth of colorectal cancer cells through the ESR2/PI3K/AKT signalling pathway. Pharmaceuticals (Basel) 17, 43. https://doi.org/10.3390/ph17010043
- Martínez-Limón, A., Joaquin, M., Caballero, M., Posas, F. and de Nadal, E. (2020) The p38 pathway: from biology to cancer therapy. Int. J. Mol. Sci. 21, 1913.
- Miller, K. D., Nogueira, L., Devasia, T., Mariotto, A. B., Yabroff, K. R., Jemal, A., Kramer, J. and Siegel, R. L. (2022) Cancer treatment and survivorship statistics, 2022. CA Cancer J. Clin. 72, 409-436.
- Murugan, A. K. (2019) mTOR: role in cancer, metastasis and drug resistance. Semin. Cancer Biol. 59, 92-111. https://doi.org/10.1016/j.semcancer.2019.07.003
- Newsholme, P., Cruzat, V. F., Keane, K. N., Carlessi, R. and de Bittencourt, P. I., Jr. (2016) Molecular mechanisms of ROS production and oxidative stress in diabetes. Biochem. J. 473, 4527-4550. https://doi.org/10.1042/BCJ20160503C
- Obrador, E., Liu-Smith, F., Dellinger, R. W., Salvador, R., Meyskens, F. L. and Estrela, J. M. (2019) Oxidative stress and antioxidants in the pathophysiology of malignant melanoma. Biol. Chem. 400, 589-612. https://doi.org/10.1515/hsz-2018-0327
- Panwar, V., Singh, A., Bhatt, M., Tonk, R. K., Azizov, S., Raza, A. S., Sengupta, S., Kumar, D. and Garg, M. (2023) Multifaceted role of mTOR (mammalian target of rapamycin) signaling pathway in human health and disease. Signal Transduct. Target. Ther. 8, 375.
- Peng, F., Du, Q., Peng, C., Wang, N., Tang, H., Xie, X., Shen, J. and Chen, J. (2015) A review: the pharmacology of isoliquiritigenin. Phytother. Res. 29, 969-977. https://doi.org/10.1002/ptr.5348
- Perillo, B., Di Donato, M., Pezone, A., Di Zazzo, E., Giovannelli, P., Galasso, G., Castoria, G. and Migliaccio, A. (2020) ROS in cancer therapy: the bright side of the moon. Exp. Mol. Med. 52, 192-203. https://doi.org/10.1038/s12276-020-0384-2
- Phan, T., Zhang, X. H., Rosen, S. and Melstrom, L. G. (2023) P38 kinase in gastrointestinal cancers. Cancer Gene Ther. 30, 1181-1189. https://doi.org/10.1038/s41417-023-00622-1
- Raut, P. K. and Park, P. H. (2020) Globular adiponectin antagonizes leptin-induced growth of cancer cells by modulating inflammasomes activation: critical role of HO-1 signaling. Biochem. Pharmacol. 180, 114186. https://doi.org/10.1016/j.bcp.2020.114186
- Redza-Dutordoir, M. and Averill-Bates, D. A. (2016) Activation of apoptosis signalling pathways by reactive oxygen species. Biochim. Biophys. Acta 1863, 2977-2992. https://doi.org/10.1016/j.bbamcr.2016.09.012
- Shakya, R., Byun, M. R., Joo, S. H., Chun, K. S. and Choi, J. S. (2023) Domperidone exerts antitumor activity in triple-negative breast cancer cells by modulating reactive oxygen species and JAK/STAT3 signaling. Biomol. Ther. (Seoul) 31, 692-699. https://doi.org/10.4062/biomolther.2023.173
- Siegel, R. L., Miller, K. D., Fuchs, H. E. and Jemal, A. (2022) Cancer statistics, 2022. CA Cancer J. Clin. 72, 7-33.
- Siegel, R. L., Miller, K. D., Wagle, N. S. and Jemal, A. (2023) Cancer statistics, 2023. CA Cancer J. Clin. 73, 17-48.
- Sim, S. J., Jang, J. H., Choi, J. S. and Chun, K. S. (2024) Domperidone, a dopamine receptor D2 antagonist, induces apoptosis by inhibiting the ERK/STAT3-mediated pathway in human colon cancer HCT116 cells. Biomol. Ther. (Seoul) 32, 568-576. https://doi.org/10.4062/biomolther.2024.048
- Son, Y., Cheong, Y. K., Kim, N. H., Chung, H. T., Kang, D. G. and Pae, H. O. (2011) Mitogen-activated protein kinases and reactive oxygen species: how can ROS activate MAPK pathways? J. Signal. Transduct. 2011, 792639. https://doi.org/10.1155/2011/792639
- Song, H. M., Park, G. H., Eo, H. J., Lee, J. W., Kim, M. K., Lee, J. R., Lee, M. H., Koo, J. S. and Jeong, J. B. (2015) Anti-proliferative effect of naringenin through p38-dependent downregulation of cyclin D1 in human colorectal cancer cells. Biomol. Ther. (Seoul) 23, 339-344. https://doi.org/10.4062/biomolther.2015.024
- Song, L., Luo, Y., Li, S., Hong, M., Wang, Q., Chi, X. and Yang, C. (2020) ISL induces apoptosis and autophagy in hepatocellular carcinoma via downregulation of PI3K/AKT/mTOR pathway in vivo and in vitro. Drug Des. Devel. Ther. 14, 4363-4376. https://doi.org/10.2147/DDDT.S270124
- Tang, L., Li, J., Fu, W., Wu, W. and Xu, J. (2019) Suppression of FADS1 induces ROS generation, cell cycle arrest, and apoptosis in melanocytes: implications for vitiligo. Aging (Albany N.Y.) 11, 11829-11843. https://doi.org/10.18632/aging.102452
- Tian, T., Sun, J., Wang, J., Liu, Y. and Liu, H. (2018) Isoliquiritigenin inhibits cell proliferation and migration through the PI3K/AKT signaling pathway in A549 lung cancer cells. Oncol. Lett. 16, 6133-6139.
- Villalpando-Rodriguez, G. E. and Gibson, S. B. (2021) Reactive oxygen species (ROS) regulates different types of cell death by acting as a rheostat. Oxid. Med. Cell. Longev. 2021, 9912436.
- Wang, T. T., Chen, Z. Z., Xie, P., Zhang, W. J., Du, M. Y., Liu, Y. T., Zhu, H. Y. and Guo, Y. S. (2019) Isoliquiritigenin suppresses the proliferation and induced apoptosis via miR-32/LATS2/Wnt in nasopharyngeal carcinoma. Eur. J. Pharmacol. 856, 172352.
- Wang, X. (2001) The expanding role of mitochondria in apoptosis. Genes Dev. 15, 2922-2933.
- Wang, Z. F., Liu, J., Yang, Y. A. and Zhu, H. L. (2020) A review: the anti-inflammatory, anticancer and antibacterial properties of four kinds of Licorice flavonoids isolated from Licorice. Curr. Med. Chem. 27, 1997-2011. https://doi.org/10.2174/0929867325666181001104550
- Wu, C. H., Chen, H. Y., Wang, C. W., Shieh, T. M., Huang, T. C., Lin, L. C., Wang, K. L. and Hsia, S. M. (2016) Isoliquiritigenin induces apoptosis and autophagy and inhibits endometrial cancer growth in mice. Oncotarget 7, 73432-73447. https://doi.org/10.18632/oncotarget.12369
- Xu, X., Zhi, T., Chao, H., Jiang, K., Liu, Y., Bao, Z., Fan, L., Wang, D., Li, Z., Liu, N. and Ji, J. (2018) ERK1/2/mTOR/Stat3 pathway-mediated autophagy alleviates traumatic brain injury-induced acute lung injury. Biochim. Biophys. Acta Mol. Basis Dis. 1864, 1663-1674. https://doi.org/10.1016/j.bbadis.2018.02.011
- Yang, H., Villani, R. M., Wang, H., Simpson, M. J., Roberts, M. S., Tang, M. and Liang, X. (2018) The role of cellular reactive oxygen species in cancer chemotherapy. J. Exp. Clin. Cancer Res. 37, 266. https://doi.org/10.1186/s13046-018-0909-x
- Ye, T., Zhu, S., Zhu, Y., Feng, Q., He, B., Xiong, Y., Zhao, L., Zhang, Y., Yu, L. and Yang, L. (2016) Cryptotanshinone induces melanoma cancer cells apoptosis via ROS-mitochondrial apoptotic pathway and impairs cell migration and invasion. Biomed. Pharmacother. 82, 319-326. https://doi.org/10.1016/j.biopha.2016.05.015
- Yu, D., Liu, X., Zhang, G., Ming, Z. and Wang, T. (2018) Isoliquiritigenin inhibits cigarette smoke-induced COPD by attenuating inflammation and oxidative stress via the regulation of the Nrf2 and NF-kappaB signaling pathways. Front. Pharmacol. 9, 1001. https://doi.org/10.3389/fphar.2018.01001
- Yu, M., Pan, Q., Li, W., Du, T., Huang, F., Wu, H., He, Y., Wu, X. and Shi, H. (2023) Isoliquiritigenin inhibits gastric cancer growth through suppressing GLUT4 mediated glucose uptake and inducing PDHK1/PGC-1α mediated energy metabolic collapse. Phytomedicine 121, 155045. https://doi.org/10.1016/j.phymed.2023.155045
- Zhang, J., Wang, X., Vikash, V., Ye, Q., Wu, D., Liu, Y. and Dong, W. (2016) ROS and ROS-mediated cellular signaling. Oxid. Med. Cell. Longev. 2016, 4350965.
- Zhang, X., Yeung, E. D., Wang, J., Panzhinskiy, E. E., Tong, C., Li, W. and Li, J. (2010) Isoliquiritigenin, a natural anti-oxidant, selectively inhibits the proliferation of prostate cancer cells. Clin. Exp. Pharmacol. Physiol. 37, 841-847. https://doi.org/10.1111/j.1440-1681.2010.05395.x
- Zhang, Z., Chen, W. Q., Zhang, S. Q., Bai, J. X., Liu, B., Yung, K. K. and Ko, J. K. (2022) Isoliquiritigenin inhibits pancreatic cancer progression through blockade of p38 MAPK-regulated autophagy. Phytomedicine 106, 154406. https://doi.org/10.1016/j.phymed.2022.154406
- Zhou, J., Wulfkuhle, J., Zhang, H., Gu, P., Yang, Y., Deng, J., Margolick, J. B., Liotta, L. A., Petricoin, E., 3rd and Zhang, Y. (2007) Activation of the PTEN/mTOR/STAT3 pathway in breast cancer stem-like cells is required for viability and maintenance. Proc. Natl. Acad. Sci. U. S. A. 104, 16158-16163. https://doi.org/10.1073/pnas.0702596104