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Contents 1

Comparison of the cytotoxicity of bisphenol A and its analogs on human placental BeWo cells / Mi Jin Kim ; Ah-Ra Jo ; Ji-Young Kim ; Mi-Jin An ; Geun-Seup Shin ; Hyun-Min Lee ; Jinho Kim ; Jinhong Park ; Chul-Hong Kim ; Jung-Woong Kim 1

Abstract 1

Introduction 1

Material and methods 2

Results 3

Discussion 7

Author contributions 9

References 10

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권호기사 목록 테이블로 기사명, 저자명, 페이지, 원문, 기사목차 순으로 되어있습니다.
기사명 저자명 페이지 원문 목차
MiR-601 inhibited small cell lung cancer progression by modulating SIRT1 Hao Ding, Chenhu Gong, Zhihong Zhang, Hui Xu, Chunping Ma p. 415-424

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MiR-370-3p aggravates blood–brain barrier injury and neuron apoptosis by targeting SMURF1 to activate the TLR4/MyD88/NF-κB signaling in sepsis-associated encephalopathy Neng Wang, Dan Zhong, Jie Lin, Mei Ye, Yu Chen, Lili Wang, Mei Chen, Cong Luo p. 425-436

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Anticancer activity of herbal formula Jisilhaebaekgyeji-Tang against human breast cancer cells and its mechanism Sang Kyu Jeon, Su Mi Park, Jung Yun Ahn, Ok Hyeon Kim, Young Woo Kim, Kwang-Il Park, Sun-Dong Park, Ju-Hee Lee p. 437-451

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CircBLNK regulates tumor proliferation and apoptosis by miR-578/ING5 axis in non-small cell lung cancer Ping Li, Liuyi Zou, Zuojun Luo, Yuhua Lu, Shuang Yu, Yujun Zhu, Yong Xie p. 453-462

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SSX2IP as a novel prognosis biomarker plays an important role in the development of breast cancer Xianfu Liu, Min Tao p. 463-472

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NEAT1 promotes keratinocyte migration and proliferation during wound healing by regulating miR-26a-5p/LGR4 axis Lan Zhang, Rong Tian, Kui Wang p. 473-481

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Iridin abrogates LPS-induced inflammation in L6 skeletal muscle cells by inhibiting NF-κB and MAPK signaling pathway Pritam Bhagwan Bhosale, Sang Eun Ha, Hun Hwan Kim, Abuyaseer Abusaliya, Min Yeong Park, Gon Sup Kim, Jin-A. Kim p. 483-490

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FBXO22 promotes cell proliferation and inhibits autophagy in HPV-associated cervical cancer by inactivating the LKB1/AMPK pathway Fuxian Gao, Chunxiao Wang, Jianghai Ji, Wenjuan Li p. 491-498

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Comparative RNA-seq analysis and ceRNA network of genistein-treated GT1-7 neurons Jingyuan Xiong, Ye Tian, Guochen Ma, Aru Ling, Shufang Shan, Guo Cheng p. 499-507

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Intestine epithelial cell-derived extracellular vesicles alleviate inflammation induced by Clostridioides difficile TcdB through the activity of TGF-β1 Shuangshuang Wan, Guangzhong Song, Hui Hu, Yaqing Xu, Peng Zeng, Shan Lin, Jun Yang, Jinqin Jiang, Xiaojun Song, Yongneng Luo, Dazhi Jin p. 509-519

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Concurrent upregulation of immune checkpoint molecule genes in colorectal cancer Hui-Jae Bang, Joon Hyung Sohn, Soo-Ki Kim, Cheol Su Kim, Mee-Yon Cho, BoRa Kim, Sanghyun An, Kwangmin Kim, Youngwan Kim p. 521-529

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KLF9 promotes autophagy and apoptosis in T-cell acute lymphoblastic leukemia cells by inhibiting AKT/mTOR signaling pathway Jie Zhao, Shaolong He, Chenhuan Xiang, Shaoli Zhang, Xinyue Chen, Xinyi Lu, Qiong Yao, Liping Yang, Liangming Ma, Weiwei Tian p. 531-538

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Beta-naphthoflavone increases the differentiation of osteoblasts and suppresses adipogenesis in human adipose derived stem cells involving STAT3 pathway Ming Lu, Min Li, Tao Luo, Yongsui Li, Mingxin Wang, Huashi Xue, Mengchen Zhang, Qiu Chen p. 539-549

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Illuminating the hepatotoxic mechanism of norcantharidin in rats using metabolomics analysis Weina Cheng, Qihong Chen, Xiaoning Wang, Liu Liu, Xiaofei Li, Cancan Duan, Jianyong Zhang p. 551-564

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circLETM1 upregulates KRT80 via adsorbing miR-143-3p and promotes the progression of colorectal cancer Hua Li, Junyu Guo, Zhongwei Qin, Mingwei Wei, Houji Guo, Fuda Huang p. 565-577

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Circular RNA circ_0000877 serves as a miR-671-5p sponge to regulate diffuse large B-cell lymphoma development via HK2 Weilun Zhou, Cuiping Wu, Jiao Wang p. 579-590

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Matrine promotes trophoblast invasion and reduces inflammation via miR-19a-3p to prevent preeclampsia Weina Yang, Qian Kang, Chunlei Li, Shuchun Bo, Yue Wang p. 591-599

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Comparison of the cytotoxicity of bisphenol A and its analogs on human placental BeWo cells Mi Jin Kim, Ah-Ra Jo, Ji-Young Kim, Mi-Jin An, Geun-Seup Shin, Hyun-Min Lee, Jinho Kim, Jinhong Park, Chul-Hong Kim, Jung-Woong Kim p. 601-611

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Identification of chromosomal type II toxin–antitoxin system from plant pathogenic Pseudomonas cichorii JBC 1 Wonho Choi, Jae-hui Kim, Ju Seok Lee, Jung-Ho Park p. 613-620

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3D structural analysis of aptamer and diagnostic platforms for detecting hepatocellular carcinoma Woo-Ri Shin, Dae-Young Park, Hyun-Ju Um, Gna Ahn, Sang Yong Kim, Ji-Young Ahn, Yang-Hoon Kim p. 621-634

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참고문헌 (42건) : 자료제공( 네이버학술정보 )

참고문헌 목록에 대한 테이블로 번호, 참고문헌, 국회도서관 소장유무로 구성되어 있습니다.
번호 참고문헌 국회도서관 소장유무
1 Adriani W et al (2003) Altered profiles of spontaneous novelty seeking, impulsive behavior, and response to D-amphetamine in rats perinatally exposed to bisphenol A. Environ Health Perspect 111(4):395–401 미소장
2 Benachour N, Aris A (2009) Toxic effects of low doses of Bisphenol-A on human placental cells. Toxicol Appl Pharmacol 241(3):322–328 미소장
3 Bolli A et al (2008) Laccase treatment impairs bisphenol A-induced cancer cell proliferation affecting estrogen receptor alpha-dependent rapid signals. IUBMB Life 60(12):843–852 미소장
4 Carr R et al (2003) Effect of neonatal rat bisphenol a exposure on performance in the Morris water maze. J Toxicol Environ Health A 66(21):2077–2088 미소장
5 erta D et al (2011) Environment and women’s reproductive health. Hum Reprod Update 17(3):418–433 미소장
6 Delfosse V et al (2012) Structural and mechanistic insights into bisphenols action provide guidelines for risk assessment and discovery of bisphenol A substitutes. Proc Natl Acad Sci USA 109(37):14930–14935 미소장
7 Diamanti-Kandarakis E et al (2009) Endocrine-disrupting chemicals: an Endocrine Society scientific statement. Endocr Rev 30(4):293–342 미소장
8 Dong YD et al (2020) Abnormal differentiation of regulatory T cells and Th17 cells induced by perinatal bisphenol A exposure in female offspring mice. Mol Cell Toxicol 16(2):167–174 미소장
9 Ehrlich S et al (2012) Urinary bisphenol A concentrations and implantation failure among women undergoing in vitro fertilization. Environ Health Perspect 120(7):978–983 미소장
10 Eladak S et al (2015) A new chapter in the bisphenol A story: bisphenol S and bisphenol F are not safe alternatives to this compound. Fertil Steril 103(1):11–21 미소장
11 FAO/WHO (2011) Joint Food and Agriculture Organization of the United Nations and World Health Organization (FAO/WHP) expert meeting to review toxicological and health aspects of bisphenol a: final report, including report of stakeholder meeting on Bisphenol A, 1–5 November 2010." Food and Agriculture Organization of the United Nations and World Health Organization, Ottawa, Canada (2011) 미소장
12 Feng Y et al (2016) Effects of bisphenol analogues on steroidogenic gene expression and hormone synthesis in H295R cells. Chemosphere 147:9–19 미소장
13 George VC, Rupasinghe HPV (2018) DNA damaging and apoptotic potentials of Bisphenol A and Bisphenol S in human bronchial epithelial cells. Environ Toxicol Pharmacol 60:52–57 미소장
14 Gingrich J et al (2018) Gestational bisphenol S impairs placental endocrine function and the fusogenic trophoblast signaling pathway. Arch Toxicol 92(5):1861–1876 미소장
15 Gore AC et al (2015) EDC-2: the endocrine society’s second scientific statement on endocrine-disrupting chemicals. Endocr Rev 36(6):E1–E150 미소장
16 Grignard E et al (2012) Weak estrogenic transcriptional activities of Bisphenol A and Bisphenol S. Toxicol in Vitro 26(5):727–731 미소장
17 Ikezuki Y et al (2002) Determination of bisphenol A concentrations in human biological fluids reveals significant early prenatal exposure. Hum Reprod 17(11):2839–2841 미소장
18 Jin H, Audus KL (2005) Effect of bisphenol A on drug efflux in BeWo, a human trophoblast-like cell line. Placenta 26 Suppl A:S96–S103 미소장
19 Kim JY et al (2017) Effects of bisphenol compounds on the growth and epithelial mesenchymal transition of MCF-7 CV human breast cancer cells. J Biomed Res 31(4):358–369 미소장
20 Kim MJ et al (2019) Propylparaben induces apoptotic cell death in human placental BeWo cells via cell cycle arrest and enhanced caspase-3 activity. Mol Cell Toxicol 16(1):83–92 미소장
21 Kim JY et al (2020a) Methylparaben induces cell-cycle arrest and caspase-3-mediated apoptosis in human placental BeWo cells. Mol Cell Toxicol 16(4):409–418 미소장
22 Kim MJ et al (2020b) Exposure to mercury induced early apoptotic signals in human placental BeWo cells through alteration of cell cycle regulation. Mol Cell Toxicol 16(4):419–429 미소장
23 Kim JY et al (2021) The cytotoxic effects of bisphenol A alternatives in human lung fibroblast MRC5 cells. Mol Cell Toxicol 17(3):267–276 미소장
24 Kitamura S et al (2005) Comparative study of the endocrine-disrupting activity of bisphenol A and 19 related compounds. Toxicol Sci 84(2):249–259 미소장
25 Kuruto-Niwa R et al (2007) Measurement of bisphenol A concentrations in human colostrum. Chemosphere 66(6):1160–1164 미소장
26 Lei B et al (2018) Low-concentration BPAF- and BPF-induced cell biological effects are mediated by ROS in MCF-7 breast cancer cells. Environ Sci Pollut Res Int 25(4):3200–3208 미소장
27 Michalowicz J et al (2015) Bisphenol A and its analogs induce morphological and biochemical alterations in human peripheral blood mononuclear cells (in vitro study). Toxicol Vitro 29(7):1464–1472 미소장
28 Molina-Molina JM et al (2013) In vitro study on the agonistic and antagonistic activities of bisphenol-S and other bisphenol-A congeners and derivatives via nuclear receptors. Toxicol Appl Pharmacol 272(1):127–136 미소장
29 Oehlmann J et al (2009) A critical analysis of the biological impacts of plasticizers on wildlife. Philos Trans R Soc Lond B Biol Sci 364(1526):2047–2062 미소장
30 Park C et al (2020) The mixture effects of bisphenol derivatives on estrogen receptor and androgen receptor. Environ Pollut 260:114036 미소장
31 Peyre L et al (2014) Comparative study of bisphenol A and its analogue bisphenol S on human hepatic cells: a focus on their potential involvement in nonalcoholic fatty liver disease. Food Chem Toxicol 70:9–18 미소장
32 Ptak A et al (2011) Effect of bisphenol-A on the expression of selected genes involved in cell cycle and apoptosis in the OVCAR-3 cell line. Toxicol Lett 202(1):30–35 미소장
33 Qiu W et al (2018) Immunotoxicity of bisphenol S and F are similar to that of bisphenol A during zebrafish early development. Chemosphere 194:1–8 미소장
34 Qiu W et al (2019) The occurrence, potential toxicity, and toxicity mechanism of bisphenol S, a substitute of bisphenol A: A critical review of recent progress. Ecotoxicol Environ Saf 173:192–202 미소장
35 Ricupito A et al (2009) Effect of bisphenol A with or without enzyme treatment on the proliferation and viability of MCF-7 cells. Environ Int 35(1):21–26 미소장
36 Rochester JR (2013) Bisphenol A and human health: a review of the literature. Reprod Toxicol 42:132–155 미소장
37 Rochester JR, Bolden AL (2015) Bisphenol S and F: a systematic review and comparison of the hormonal activity of Bisphenol A substitutes. Environ Health Perspect 123(7):643–650 미소장
38 Rubin BS (2011) Bisphenol A: an endocrine disruptor with widespread exposure and multiple effects. J Steroid Biochem Mol Biol 127(1–2):27–34 미소장
39 Schonfelder G et al (2002) Parent bisphenol A accumulation in the human maternal-fetal-placental unit. Environ Health Perspect 110(11):A703-707 미소장
40 Vandenberg LN et al (2010) Urinary, circulating, and tissue biomonitoring studies indicate widespread exposure to bisphenol A. Environ Health Perspect 118(8):1055–1070 미소장
41 Wang ZY et al (2015) Effect of Bisphenol A on invasion ability of human trophoblastic cell line BeWo. Int J Clin Exp Pathol 8(11):14355–14364 미소장
42 Zhang XY et al (2020) Adverse effects of subchronic exposure to cooking oil fumes on the gonads and the GPR30-mediated signaling pathway in female rats. Mol Cell Toxicol 16(1):13–24 미소장

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