Germacrone, A Novel and Safe Anticancer Agent from Genus Curcuma: A Review of its Mechanism


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Germacrone, a kind of natural sesquiterpenoid compound, has been reported to exhibit many pharmacological properties, especially the anticancer effect. Many in vitro experiments have been performed on various cancer cell lines, trying to explore their anticancer mechanism. Aiming at investigating the anticancer effect of germacrone, this article reviews the extant information on existing literature about germacrone-related studies. The anticancer mechanisms and clinical usages of germacrone are summarized. Literature databases (such as PubMed and CNKI) are used to search the current studies and experimental research about the anticancer effect information of germacrone. Anticancer mechanism of germacrone includes cell cycle arrest inducing, programmed cell death (apoptosis, autophagy, pyroptosis and ferroptosis) inducing, and estrogen-related genes mediating. Structural modification and analogue design are worthy of further study in the future

作者简介

Guanhua Lou

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Yan Huang

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Yu Wang

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Shiyun Chen

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Chang Liu

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Ying Li

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

Email: info@benthamscience.net

Jianan Feng

Institute of Traditional Chinese Medicine, Sichuan Academy of Traditional Chinese Medicine

编辑信件的主要联系方式.
Email: info@benthamscience.net

参考

  1. Wu, T.; Yin, F.; Kong, H.; Peng, J. Germacrone attenuates cerebral ischemia/reperfusion injury in rats via antioxidative and antiapoptotic mechanisms. J. Cell. Biochem., 2019, 120(11), 18901-18909. doi: 10.1002/jcb.29210 PMID: 31318092
  2. Chen, Q.F.; Wang, G.; Tang, L.Q.; Yu, X.W.; Li, Z.F.; Yang, X.F. Effect of germacrone in alleviating HUVECs damaged by H2O2-induced oxidative stress. Zhongguo Zhongyao Zazhi, 2017, 42(18), 3564-3571. PMID: 29218943
  3. Zhang, J.; Yuan, L.; Wang, S.; Liu, J.; Bi, H.; Chen, G.; Li, J.; Chen, L. Germacrone protects against oxygen-glucose deprivation/reperfusion injury by inhibiting autophagy processes in PC12 cells. BMC Complement. Med. Ther., 2020, 20(1), 77-86. doi: 10.1186/s12906-020-2865-1 PMID: 32145743
  4. Pan, J.; Miao, D.; Chen, L. Germacrone reverses adriamycin resistance in human chronic myelogenous leukemia K562/ADM cells by suppressing MDR1 gene/P-glycoprotein expression. Chem. Biol. Interact., 2018, 288, 32-37. doi: 10.1016/j.cbi.2018.04.012 PMID: 29655913
  5. He, W.; Zhai, X.; Su, J.; Ye, R.; Zheng, Y.; Su, S. Antiviral activity of germacrone against pseudorabies virus in vitro. Pathogens, 2019, 8(4), 258-271. doi: 10.3390/pathogens8040258 PMID: 31766701
  6. Liao, Q.; Qian, Z.; Liu, R.; An, L.; Chen, X. Germacrone inhibits early stages of influenza virus infection. Antiviral Res., 2013, 100(3), 578-588. doi: 10.1016/j.antiviral.2013.09.021 PMID: 24095670
  7. Chen, Y.; Dong, Y.; Jiao, Y.; Hou, L.; Shi, Y.; Gu, T.; Zhou, P.; Shi, Z.; Xu, L.; Wang, C. In vitro antiviral activity of germacrone against porcine parvovirus. Arch. Virol., 2015, 160(6), 1415-1420. doi: 10.1007/s00705-015-2393-3 PMID: 25813663
  8. Wang, Z.; Zhuo, F.; Chu, P.; Yang, X.; Zhao, G. Germacrone alleviates collagen-induced arthritis via regulating Th1/Th2 balance and NF-κB activation. Biochem. Biophys. Res. Commun., 2019, 518(3), 560-564. doi: 10.1016/j.bbrc.2019.08.084 PMID: 31451221
  9. Galisteo Pretel, A.; Pérez Del Pulgar, H.; Guerrero de León, E.; López-Pérez, J.L.; Olmeda, A.S.; Gonzalez-Coloma, A.; Barrero, F. A.; Quílez Del Moral, J.F. Germacrone derivatives as new insecticidal and acaricidal compounds: A structure-activity relationship. Molecules, 2019, 24(16), 2898. doi: 10.3390/molecules24162898 PMID: 31404973
  10. Sun, Y.; Li, L.; Wu, J.; Gong, B.; Liu, H. Germacrone cooperates with dexmedetomidine to alleviate high fat diet induced type 2 diabetes mellitus via upregulating AMPKα1 expression. Exp. Ther. Med., 2019, 18(5), 3514-3524. doi: 10.3892/etm.2019.7990 PMID: 31602228
  11. Jin, J.; Wang, Y.; Zheng, D.; Liang, M.; He, Q. A novel identified circular RNA, mmu_mmu_circRNA_0000309, involves in germacrone-mediated improvement of diabetic nephropathy through regulating ferroptosis by targeting miR-188-3p/GPX4 signaling axis. Antioxid. Redox Signal., 2022, 36(10-12), 740-759. doi: 10.1089/ars.2021.0063 PMID: 34913724
  12. Guo, Y.R.; Choung, S.Y. Germacrone attenuates hyperlipidemia and improves lipid metabolism in high-fat diet-induced obese C57BL/6J mice. J. Med. Food, 2017, 20(1), 46-55. doi: 10.1089/jmf.2016.3811 PMID: 28098516
  13. Zhuang, S.; Liu, B.; Guo, S.; Xue, Y.; Wu, L.; Liu, S.; Zhang, C.; Ni, X. Germacrone alleviates neurological deficits following traumatic brain injury by modulating neuroinflammation and oxidative stress. BMC Complement. Med. Ther., 2021, 21(1), 6-15. doi: 10.1186/s12906-020-03175-0 PMID: 33402180
  14. Lin, M.; Li, P.; Liu, W.; Niu, T.; Huang, L. Germacrone alleviates okadaic acid-induced neurotoxicity in PC12 cells via M1 muscarinic receptor-mediated Galphaq (Gq)/phospholipase C beta (PLCβ)/protein kinase C (PKC) signaling. Bioengineered, 2022, 13(3), 4898-4910. doi: 10.1080/21655979.2022.2036918 PMID: 35156515
  15. Riaz, A.; Rasul, A.; Kanwal, N.; Hussain, G.; Shah, M.A.; Sarfraz, I.; Ishfaq, R.; Batool, R.; Rukhsar, F. Adem, Ş. Germacrone: A potent secondary metabolite with therapeutic potential in metabolic diseases, cancer and viral infections. Curr. Drug Metab., 2020, 21(14), 1079-1090. doi: 10.2174/1389200221999200728144801 PMID: 32723267
  16. Li, E.; Gao, Y.; Mou, L.; Zhang, Z. Anticancer activity of Germacrone terpenoid in human osteosarcoma cells is mediated via autophagy induction, cell cycle disruption, downregulating the cell cycle regulatory protein expressions and cell migration inhibition. Acta Biochim. Pol., 2022, 69(2), 305-308. doi: 10.18388/abp.2020_5712 PMID: 35468267
  17. Li, Z.; Wang, Z.; Dong, F.; Shi, W.; Dai, W.; Zhao, J.; Li, Q.; Fang, Z.; Ren, L.; Liu, T.; Wei, Z.; Mou, W.; Lin, L.; Yang, Y.; Xiao, X.; Ma, L.; Bai, Z. Germacrone attenuates hepatic stellate cells activation and liver fibrosis via regulating multiple signaling pathways. Front. Pharmacol., 2021, 12(12), 745561. doi: 10.3389/fphar.2021.745561 PMID: 34675811
  18. Ognjanov, I.; Ivanov, D.; Herout, V.; Horák, M.; Plíva, J.; Šorm, F. On terpenes. LXXXVIII. The structure of germacrone, the crystalline constituent of Bulgarian zdravets oil. Collect. Czech. Chem. Commun., 1958, 23(11), 2033-2045. doi: 10.1135/cccc19582033
  19. Fang, X.; Tan, T.; Gao, B.; Zhao, Y.; Liu, T.; Xia, Q. Germacrone regulates HBXIP-Mediated cell cycle, apoptosis and promotes the formation of autophagosomes to inhibit the proliferation of gastric cancer cells. Front. Oncol., 2020, 10, 537322. doi: 10.3389/fonc.2020.537322 PMID: 33244453
  20. Zhang, R.; Hao, J.; Guo, K.; Liu, W.; Yao, F.; Wu, Q.; Liu, C.; Wang, Q.; Yang, X. Germacrone inhibits cell proliferation and induces apoptosis in human esophageal squamous cell carcinoma cells. BioMed Res. Int., 2020, 2020, 1-13. doi: 10.1155/2020/7643248 PMID: 32071920
  21. Zhao, Y.; Cai, J.; Shi, K.; Li, H.; Du, J.; Hu, D.; Liu, Z.; Wang, W. Germacrone induces lung cancer cell apoptosis and cell cycle arrest via the Akt/MDM2/p53 signaling pathway. Mol. Med. Rep., 2021, 23(6), 452-460. doi: 10.3892/mmr.2021.12091 PMID: 33880579
  22. Serpa, G.A.M.; Gómez, H.C.; Velásquez-Cock, J.A.; Vélez, A.L.; Gañán Rojo, P.; Velásquez, A.M.; Zuluaga Gallego, R. The nanotech potential of turmeric (Curcuma longa L.) in food technology: A review. Crit. Rev. Food Sci. Nutr., 2020, 60(11), 1842-1854. doi: 10.1080/10408398.2019.1604490 PMID: 31017458
  23. Karlowicz-Bodalska, K.; Han, S.; Freier, J.; Smolenski, M.; Bodalska, A. Curcuma longa as medicinal herb in the treatment of diabet- ic complications. Acta Pol. Pharm., 2017, 74(2), 605-610. PMID: 29624265
  24. Kamazeri, T.S.A.T.; Samah, O.A.; Taher, M.; Susanti, D.; Qaralleh, H. Antimicrobial activity and essential oils of Curcuma aeruginosa, Curcuma mangga, and Zingiber cassumunar from Malaysia. Asian Pac. J. Trop. Med., 2012, 5(3), 202-209. doi: 10.1016/S1995-7645(12)60025-X PMID: 22305785
  25. Burapan, S.; Kim, M.; Paisooksantivatana, Y.; Eser, B.E.; Han, J. Thai Curcuma Species: Antioxidant and bioactive compounds. Foods, 2020, 9(9), 1219. doi: 10.3390/foods9091219 PMID: 32887356
  26. Kuroyanagi, M.; Ueno, A.; Ujiie, K.; Sato, S. Structures of sesquiterpenes from Curcuma aromatica Salisb. Chem. Pharm. Bull., 1987, 35(1), 53-59. doi: 10.1248/cpb.35.53
  27. Dosoky, N.; Setzer, W. Chemical composition and biological activities of essential oils of Curcuma species. Nutrients, 2018, 10(9), 1196-1237. doi: 10.3390/nu10091196 PMID: 30200410
  28. Zhang, L.; Yang, Z.; Huang, Z.; Zhao, M.; Li, P.; Zhou, W.; Zhang, K.; Zheng, X.; Lin, L.; Tang, J.; Fang, Y.; Du, Z. Variation in essential oil and bioactive compounds of Curcuma kwangsiensis collected from natural habitats. Chem. Biodivers., 2017, 14(7), e1700020. doi: 10.1002/cbdv.201700020 PMID: 28398606
  29. Yin, G.P.; Zhang, Q.Z.; An, Y.W.; Zhu, J.J.; Wang, Z.M. Advance in chemical constituents and pharmacological activity of Curcuma wenyujin. Zhongguo Zhongyao Zazhi, 2012, 37(22), 3354-3360. PMID: 23373201
  30. Siddique, H.; Pendry, B.; Rahman, M.M. Terpenes from Zingiber montanum and their screening against multi-drug resistant and methicillin resistant Staphylococcus aureus. Molecules, 2019, 24(3), 385-394. doi: 10.3390/molecules24030385 PMID: 30678230
  31. Huong, L.T.; Chung, N.T.; Huong, T.T.; Sam, L.N.; Hung, N.H.; Ogunwande, I.A.; Dai, D.N.; Linh, L.D.; Setzer, W.N. Essential oils of Zingiber species from vietnam: Chemical compositions and biological activities. Plants, 2020, 9(10), 1269. doi: 10.3390/plants9101269 PMID: 32993137
  32. Liu, Y.; Liu, J.; Zhang, Y. Research progress on chemical constituents of Zingiber officinale roscoe. BioMed Res. Int., 2019, 2019, 1-21. doi: 10.1155/2019/5370823 PMID: 31930125
  33. Zeljković, S.Ć.; Tan, K.; Siljak-Yakovlev, S.; Maksimović, M. Essential oil profile, phenolic content and antioxidant activity of Geranium kikianum. Nat. Prod. Commun., 2017, 12(2), 1934578X1701200. doi: 10.1177/1934578X1701200234 PMID: 30428229
  34. Radulović N.S.; Dekić M.S.; Stojanović-Radić Z.Z.; Zoranić S.K. Geranium macrorrhizum L. (Geraniaceae) essential oil: A potent agent against Bacillus subtilis. Chem. Biodivers., 2010, 7(11), 2783-2800. doi: 10.1002/cbdv.201000100 PMID: 21072778
  35. Doss, R.P.; Luthi, R.; Hrutfiord, B.F. Germacrone, a sesquiterpene repellent to obscure root weevil from Rhododendron edgeworthii. Phytochemistry, 1980, 19(11), 2379-2380. doi: 10.1016/S0031-9422(00)91031-8
  36. Wu, L.; Wang, L.; Tian, X.; Zhang, J.; Feng, H. Germacrone exerts anti-cancer effects on gastric cancer through induction of cell cycle arrest and promotion of apoptosis. BMC Compl. Med. Ther., 2020, 20(1), 21-29. doi: 10.1186/s12906-019-2810-3 PMID: 32020876
  37. Liu, Y.; Wang, W.; Fang, B.; Ma, F.; Zheng, Q.; Deng, P.; Zhao, S.; Chen, M.; Yang, G.; He, G. Anti-tumor effect of germacrone on human hepatoma cell lines through inducing G2/M cell cycle arrest and promoting apoptosis. Eur. J. Pharmacol., 2013, 698(1-3), 95-102. doi: 10.1016/j.ejphar.2012.10.013 PMID: 23117090
  38. Liu, B.O.; Gao, Y.U.E.Q.I.U.; Wang, X.M.; Wang, Y.C.; Fu, L.I.Q.I. Germacrone inhibits the proliferation of glioma cells by promoting apoptosis and inducing cell cycle arrest. Mol. Med. Rep., 2014, 10(2), 1046-1050. doi: 10.3892/mmr.2014.2290 PMID: 24889088
  39. Zhong, Z.; Chen, X.; Tan, W.; Xu, Z.; Zhou, K.; Wu, T.; Cui, L.; Wang, Y. Germacrone inhibits the proliferation of breast cancer cell lines by inducing cell cycle arrest and promoting apoptosis. Eur. J. Pharmacol., 2011, 667(1-3), 50-55. doi: 10.1016/j.ejphar.2011.03.041 PMID: 21497161
  40. Dai, X.; Wang, D.; Zhang, J. Programmed cell death, redox imbalance, and cancer therapeutics. Apoptosis, 2021, 26(7-8), 385-414. doi: 10.1007/s10495-021-01682-0 PMID: 34236569
  41. Gerl, R.; Vaux, D.L. Apoptosis in the development and treatment of cancer. Carcinogenesis, 2004, 26(2), 263-270. doi: 10.1093/carcin/bgh283 PMID: 15375012
  42. Yu, Z.; Xu, J.; Shao, M.; Zou, J. Germacrone induces apoptosis as well as protective autophagy in human prostate cancer cells. Cancer Manag. Res., 2020, 12, 4009-4016. doi: 10.2147/CMAR.S250522 PMID: 32547235
  43. Ji, D.; Zhao, Q.; Qin, Y.; Tong, H.; Wang, Q.; Yu, M.; Mao, C.; Lu, T.; Qiu, J.; Jiang, C. Germacrone improves liver fibrosis by regulating the PI3K/AKT/mTOR signalling pathway. Cell Biol. Int., 2021, 45(9), 1866-1875. doi: 10.1002/cbin.11607 PMID: 33835632
  44. Fei, H.; Zhou, Y.; Li, R.; Yang, M.; Ma, J.; Wang, F. HBXIP, a binding protein of HBx, regulates maintenance of the G2/M phase checkpoint induced by DNA damage and enhances sensitivity to doxorubicin-induced cytotoxicity. Cell Cycle, 2017, 16(5), 468-476. doi: 10.1080/15384101.2017.1281482 PMID: 28103177
  45. Liu, Y.; Zheng, Q.; Fang, B.; Wang, W.; Ma, F.; Roshan, S.; Banafa, A.; Chen, M.; Chang, J.; Deng, X.; Li, K.; Yang, G.; He, G. Germacrone induces apoptosis in human hepatoma HepG2 cells through inhibition of the JAK2/STAT3 signalling pathway. J. Huazhong Univ. Sci. Technolog. Med. Sci., 2013, 33(3), 339-345. doi: 10.1007/s11596-013-1121-z PMID: 23771657
  46. Sadia, R. Effect of fucoidan and germacrone on cancer cell lines and the underlying mechanisms; Huazhong University of Science & Technology, 2015.
  47. Zhou, Y.; Zhang, Y.; Bai, X.; He, P. Effects of germacrone on proliferation and apoptosis in human squamous cell lung carcinoma lk2 cells. J. Chin. Med. Uni, 2013, 42(6), 508-510.
  48. Chen, X.; Pei, L.; Zhong, Z.; Guo, J.; Zhang, Q.; Wang, Y. Anti-tumor potential of ethanol extract of Curcuma phaeocaulis Valeton against breast cancer cells. Phytomedicine, 2011, 18(14), 1238-1243. doi: 10.1016/j.phymed.2011.06.017 PMID: 21795032
  49. Xie, X.H.; Zhao, H.; Hu, Y.Y.; Gu, X.D. Germacrone reverses Adriamycin resistance through cell apoptosis in multidrug-resistant breast cancer cells. Exp. Ther. Med., 2014, 8(5), 1611-1615. doi: 10.3892/etm.2014.1932 PMID: 25289068
  50. Fang, X.; Tan, T.; Gao, B.; Zhao, Y.; Liu, T.; Xia, Q. Germacrone regulates HBXIP-mediated cell cycle, apoptosis and promotes the formation of autophagosomes to inhibit the proliferation of gastric cancer cells. Front. Oncol., 2020. Available from: https://www.frontiersin.org/articles/10.3389/fonc.2020.537322/full
  51. lionsky, D.J. Autophagy revisited: A conversation with Christian de Duve. Autophagy, 2008, 4(6), 740-743. doi: 10.4161/auto.6398 PMID: 18567941
  52. Yang, Z.; Klionsky, D.J. Eaten alive: A history of macroautophagy. Nat. Cell Biol., 2010, 12(9), 814-822. doi: 10.1038/ncb0910-814 PMID: 20811353
  53. Vlahopoulos, S.; Critselis, E.; Voutsas, I.; Perez, S.; Moschovi, M.; Baxevanis, C.; Chrousos, G. New use for old drugs? Prospective targets of chloroquines in cancer therapy. Curr. Drug Targets, 2014, 15(9), 843-851. doi: 10.2174/1389450115666140714121514 PMID: 25023646
  54. Sato, K.; Tsuchihara, K.; Fujii, S.; Sugiyama, M.; Goya, T.; Atomi, Y.; Ueno, T.; Ochiai, A.; Esumi, H. Autophagy is activated in colorectal cancer cells and contributes to the tolerance to nutrient deprivation. Cancer Res., 2007, 67(20), 9677-9684. doi: 10.1158/0008-5472.CAN-07-1462 PMID: 17942897
  55. Mathew, R.; Karantza-Wadsworth, V.; White, E. Role of autophagy in cancer. Nat. Rev. Cancer, 2007, 7(12), 961-967. doi: 10.1038/nrc2254 PMID: 17972889
  56. Fang, Y.; Tian, S.; Pan, Y.; Li, W.; Wang, Q.; Tang, Y.; Yu, T.; Wu, X.; Shi, Y.; Ma, P.; Shu, Y. Pyroptosis: A new frontier in cancer. Biomed. Pharmacother., 2020, 121, 109595. doi: 10.1016/j.biopha.2019.109595 PMID: 31710896
  57. Sun, X.; Zhong, X.; Ma, W.; Feng, W.; Huang, Q.; Ma, M.; Lv, M.; Hu, R.; Han, Z.; Li, J.; Zhou, X. Germacrone induces caspase 3/GSDME activation and enhances ROS production, causing HepG2 pyroptosis. Exp. Ther. Med., 2022, 24(1), 456-468. doi: 10.3892/etm.2022.11383 PMID: 35747157
  58. Lu, B.; Chen, X.B.; Ying, M.D.; He, Q.J.; Cao, J.; Yang, B. The role of ferroptosis in cancer development and treatment response. Front. Pharmacol., 2018, 8, 992-999. doi: 10.3389/fphar.2017.00992 PMID: 29375387
  59. Cao, J.Y.; Dixon, S.J. Mechanisms of ferroptosis. Cell. Mol. Life Sci., 2016, 73(11-12), 2195-2209. doi: 10.1007/s00018-016-2194-1 PMID: 27048822
  60. Ma, S.; Henson, E.S.; Chen, Y.; Gibson, S.B. Ferroptosis is induced following siramesine and lapatinib treatment of breast cancer cells. Cell Death Dis., 2016, 7(7), e2307. doi: 10.1038/cddis.2016.208 PMID: 27441659
  61. Roh, J.L.; Kim, E.H.; Jang, H.J.; Park, J.Y.; Shin, D. Induction of ferroptotic cell death for overcoming cisplatin resistance of head and neck cancer. Cancer Lett., 2016, 381(1), 96-103. doi: 10.1016/j.canlet.2016.07.035 PMID: 27477897
  62. Eling, N.; Reuter, L.; Hazin, J.; Hamacher-Brady, A.; Brady, N.R. Identification of artesunate as a specific activator of ferroptosis in pancreatic cancer cells. Oncoscience, 2015, 2(5), 517-532. doi: 10.18632/oncoscience.160 PMID: 26097885
  63. Galmiche, A.; Chauffert, B.; Barbare, J.C. New biological perspectives for the improvement of the efficacy of sorafenib in hepatocellular carcinoma. Cancer Lett., 2014, 346(2), 159-162. doi: 10.1016/j.canlet.2013.12.028 PMID: 24380851
  64. Hong, X.; Roh, W.; Sullivan, R.J.; Wong, K.H.K.; Wittner, B.S.; Guo, H.; Dubash, T.D.; Sade-Feldman, M.; Wesley, B.; Horwitz, E.; Boland, G.M.; Marvin, D.L.; Bonesteel, T.; Lu, C.; Aguet, F.; Burr, R.; Freeman, S.S.; Parida, L.; Calhoun, K.; Jewett, M.K.; Nieman, L.T.; Hacohen, N.; Näär, A.M.; Ting, D.T.; Toner, M.; Stott, S.L.; Getz, G.; Maheswaran, S.; Haber, D.A. The lipogenic regulator SREBF2 induces Transferrin in circulating melanoma cells and suppresses ferroptosis. Cancer Discov., 2021, 11(3), 678-695. doi: 10.1158/2159-8290.CD-19-1500 PMID: 33203734
  65. Zárybnický, T.; Matoušková, P.; Skálová, L.; Boušová, I. The hepatotoxicity of alantolactone and germacrone: their influence on cholesterol and lipid metabolism in differentiated HepaRG cells. Nutrients, 2020, 12(6), 1720-1736. doi: 10.3390/nu12061720 PMID: 32521813
  66. Pedram, A.; Razandi, M.; Evinger, A.J.; Lee, E.; Levin, E.R. Estrogen inhibits ATR signaling to cell cycle checkpoints and DNA repair. Mol. Biol. Cell, 2009, 20(14), 3374-3389. doi: 10.1091/mbc.e09-01-0085 PMID: 19477925
  67. Hevir, N.; Trošt, N.; Debeljak, N.; Lanišnik Rižner, T. Expression of estrogen and progesterone receptors and estrogen metabolizing enzymes in different breast cancer cell lines. Chem. Biol. Interact., 2011, 191(1-3), 206-216. doi: 10.1016/j.cbi.2010.12.013 PMID: 21182832
  68. Hsu, L.H.; Chu, N.M.; Kao, S.H. Estrogen, estrogen receptor and lung cancer. Int. J. Mol. Sci., 2017, 18(8), 1713-1729. doi: 10.3390/ijms18081713 PMID: 28783064
  69. Nichols, M.D.; Peng, C.; Kanterewicz, B.; Day, B.W.; Hershberger, P.A. Estrogen Receptor α and β signaling in breast and lung cancers. Cancer Res., 2005, 65. Epub ahead of print
  70. Rahman, M.S.U.; Cao, J. Estrogen receptors in gastric cancer: Advances and perspectives. World J. Gastroenterol., 2016, 22(8), 2475-2482. doi: 10.3748/wjg.v22.i8.2475 PMID: 26937135
  71. Jiang, L.; Fei, H.; Yang, A.; Zhu, J.; Sun, J.; Liu, X.; Xu, W.; Yang, J.; Zhang, S. Estrogen inhibits the growth of colon cancer in mice through reversing extracellular vesicle-mediated immunosuppressive tumor microenvironment. Cancer Lett., 2021, 520, 332-343. doi: 10.1016/j.canlet.2021.08.011 PMID: 34391809
  72. Nelson, A.W.; Tilley, W.D.; Neal, D.E.; Carroll, J.S. Estrogen receptor beta in prostate cancer: friend or foe? Endocr. Relat. Cancer, 2014, 21(4), T219-T234. doi: 10.1530/ERC-13-0508 PMID: 24402043
  73. Ribeiro, J.R.; Freiman, R.N. Estrogen signaling crosstalk: Implications for endocrine resistance in ovarian cancer. J. Steroid Biochem. Mol. Biol., 2014, 143, 160-173. doi: 10.1016/j.jsbmb.2014.02.010 PMID: 24565562
  74. Blanchard, Z.; Vahrenkamp, J.M.; Berrett, K.C.; Arnesen, S.; Gertz, J. Estrogen-independent molecular actions of mutant estrogen receptor 1 in endometrial cancer. Genome Res., 2019, 29(9), 1429-1441. doi: 10.1101/gr.244780.118 PMID: 31362937
  75. Lim, M.S.; Choung, S.Y.; Jeong, K.W. Germacrone inhibits estrogen receptor α-mediated transcription in MCF-7 breast cancer cells. Phytother. Res., 2016, 30(12), 2036-2043. doi: 10.1002/ptr.5711 PMID: 27573551
  76. Szczepański, J.; Tuszewska, H.; Trotsko, N. Anticancer profile of rhodanines: Structure–activity relationship (SAR) and molecular targets-a review. Molecules, 2022, 27(12), 3750-3778. doi: 10.3390/molecules27123750 PMID: 35744873
  77. Wu, J.; Feng, Y.; Han, C.; Huang, W.; Shen, Z.; Yang, M.; Chen, W.; Ye, L. Germacrone derivatives: Synthesis, biological activity, molecular docking studies and molecular dynamics simulations. Oncotarget, 2017, 8(9), 15149-15158. doi: 10.18632/oncotarget.14832 PMID: 28148897
  78. Kochhar, K.S.; Johnson, M.E.; Volpert, O.; Iyer, A.P. Evidence for autocrine basis of transformation in NIH-3T3 cells transfected with met/HGF receptor gene. Growth Factors, 1995, 12(4), 303-313. doi: 10.3109/08977199509028968 PMID: 8930021

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