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      KCI등재 SCOPUS

      Identification of Genes Differentially Expressed in the MCF-7 CellsTreated with Mitogenic Estrogens

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      https://www.riss.kr/link?id=A104737992

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      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      Estrogens, a group of steroid compounds functioning as the primary female sex hormone, play an important role in the development and progression of breast cancer. In this study, using a novel annealing control primer-based GeneFishing PCR technology, five differentially expressed genes (DEGs), expressed using 10 nM mitogenic estrogens, 17β-estradiol (E2) and 16α-hydroxyestrone (16α-OHE1), were selected from the estrogen receptor (ER)-positive MCF-7 human breast cancer cells. The DEGs, MRPL42, TUBA1B, SSBP1, KNCT2, and RUVBL1, were identified by comparison with the known genes via direct sequencing and sequence homology search in BLAST.
      Quantitative real-time PCR data showed that two DEGs, tubulin α1b and kinetochore associated 2, were greater than 2-fold upregulated by E2 or 16α-OHE1. Both genes could be new biomarkers for the treatment and prognosis of cancers, and further study may provide insights into the molecular mechanisms underlying development and progression of breast cancer.
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      Estrogens, a group of steroid compounds functioning as the primary female sex hormone, play an important role in the development and progression of breast cancer. In this study, using a novel annealing control primer-based GeneFishing PCR technology, ...

      Estrogens, a group of steroid compounds functioning as the primary female sex hormone, play an important role in the development and progression of breast cancer. In this study, using a novel annealing control primer-based GeneFishing PCR technology, five differentially expressed genes (DEGs), expressed using 10 nM mitogenic estrogens, 17β-estradiol (E2) and 16α-hydroxyestrone (16α-OHE1), were selected from the estrogen receptor (ER)-positive MCF-7 human breast cancer cells. The DEGs, MRPL42, TUBA1B, SSBP1, KNCT2, and RUVBL1, were identified by comparison with the known genes via direct sequencing and sequence homology search in BLAST.
      Quantitative real-time PCR data showed that two DEGs, tubulin α1b and kinetochore associated 2, were greater than 2-fold upregulated by E2 or 16α-OHE1. Both genes could be new biomarkers for the treatment and prognosis of cancers, and further study may provide insights into the molecular mechanisms underlying development and progression of breast cancer.

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      참고문헌 (Reference)

      1 Saji S., "Significance of HDAC6 regulation via estrogen signaling for cell motility and prognosis in estrogen receptor-positive breast cancer" 24 : 4531-4539, 2005

      2 Martin-Lluesma S, "Role of Hec1 in spindle checkpoint signaling and kinetochore recruitment of Mad1/Mad2" 297 : 2267-2270, 2002

      3 Lewis JS, "Regulation of cell cycle and cyclins by 16α- hydroxyestrone in MCF-7 breast cancer cells" 27 : 293-307, 2001

      4 Rozen S, "Primer3 on the WWW for general users and for biologist programmers. In Bioinformatics Methods and Protocols: Methods in Molecular Biology, Krawetz S and Misener S" Humana Press 365-386, 2000

      5 Ernst M., "Phenol red mimics biological actions of estradiol: enhancement of osteoblast proliferation in vitro and of type I collagen gene expression in bone and uterus of rats in vivo" 33 : 907-914, 1989

      6 Seong Hwan Kim, "Mitogenic Estrogen Metabolites Alter the Expression of 17β-estradiol-regulated Proteins Including Heat Shock Proteins in Human MCF-7 Breast Cancer Cells" 한국분자세포생물학회 20 (20): 378-384, 2005

      7 DeLuca JG., "Kinetochore microtubule dynamics and attachment stability are regulated by Hec1" 127 : 969-982, 2006

      8 Banerjee A,, "Increased levels of tyrosinated α-, β(III)-, and β(IV)-tubulin isotypes in paclitaxel-resistant MCF-7 breast cancer cells" 293 : 598-601, 2002

      9 Fishman J., "Increased estrogen-16 a-hydroxylase activity in women with breast and endometrial cancer" 20 : 1077-1081, 1984

      10 Lee EA, "Inactivation of the mitotic checkpoint as a determinant of the efficacy of microtubule-targeted drugs in killing human cancer cells" 3 : 661-669, 2004

      1 Saji S., "Significance of HDAC6 regulation via estrogen signaling for cell motility and prognosis in estrogen receptor-positive breast cancer" 24 : 4531-4539, 2005

      2 Martin-Lluesma S, "Role of Hec1 in spindle checkpoint signaling and kinetochore recruitment of Mad1/Mad2" 297 : 2267-2270, 2002

      3 Lewis JS, "Regulation of cell cycle and cyclins by 16α- hydroxyestrone in MCF-7 breast cancer cells" 27 : 293-307, 2001

      4 Rozen S, "Primer3 on the WWW for general users and for biologist programmers. In Bioinformatics Methods and Protocols: Methods in Molecular Biology, Krawetz S and Misener S" Humana Press 365-386, 2000

      5 Ernst M., "Phenol red mimics biological actions of estradiol: enhancement of osteoblast proliferation in vitro and of type I collagen gene expression in bone and uterus of rats in vivo" 33 : 907-914, 1989

      6 Seong Hwan Kim, "Mitogenic Estrogen Metabolites Alter the Expression of 17β-estradiol-regulated Proteins Including Heat Shock Proteins in Human MCF-7 Breast Cancer Cells" 한국분자세포생물학회 20 (20): 378-384, 2005

      7 DeLuca JG., "Kinetochore microtubule dynamics and attachment stability are regulated by Hec1" 127 : 969-982, 2006

      8 Banerjee A,, "Increased levels of tyrosinated α-, β(III)-, and β(IV)-tubulin isotypes in paclitaxel-resistant MCF-7 breast cancer cells" 293 : 598-601, 2002

      9 Fishman J., "Increased estrogen-16 a-hydroxylase activity in women with breast and endometrial cancer" 20 : 1077-1081, 1984

      10 Lee EA, "Inactivation of the mitotic checkpoint as a determinant of the efficacy of microtubule-targeted drugs in killing human cancer cells" 3 : 661-669, 2004

      11 Hwang K.C., "Identification of differentially regulated genes in bovine blastocysts using an annealing control primer system" 69 : 43-51, 2004

      12 Ryu JY, "Identification of differentially expressed genes in the testis of Sprague-Dawley rats treated with di(n-butyl) phthalate" 234 : 103-112, 2007

      13 Delmas PD., "Hormone replacement therapy in the prevention and treatment of osteoporosis" 1 : S3-7, 1997

      14 Grady D., "HERS Research Group (2002) Cardiovascular disease outcomes during 6.8 years of hormone therapy: Heart and estrogen/progestin replacement study follow-up (HERS II)" Heart and estrogen/progestin replacement study follow-up(HERS II).JAMA 288,49-57. 288 : 49-57, 2002

      15 Gupta M., "Estrogenic and antiestrogenic activities of 16α- and 2-hydroxy metabolites of 17β-estradiol in MCF-7 and T47D human breast cancer cells" 67 : 413-419, 1998

      16 Clemons M., "Estrogen and the risk of breast cancer" 344 : 276-285, 2001

      17 Darbre P., "Effect of estradiol on human breast cancer cells in culture" 43 : 349-354, 1983

      18 Sengupta S., "Drug target interaction of tubulin-binding drugs in cancer therapy" 6 : 1433-1447, 2006

      19 Li L, "Development of recombinant adeno-associated virus vectors carrying small interfering RNA (shHec1)-mediated depletion of kinetochore Hec1 protein in tumor cells" 14 : 817-824, 2007

      20 Swaneck GE, "Covalent binding of the endogenous estrogen 16 a-hydroxyestrone to estradiol receptor in human breast cancer cells: characterization and intranuclear localization" 85 : 7831-7835, 1988

      21 Fishman J., "Biological properties of 16 a-hydroxyestrone: implications in estrogen physiology and pathophysiology" 51 : 611-615, 1980

      22 Kim YJ, "Annealing control primer system for identification of differentially expressed genes on agarose gels" 36 : 424-430, 2004

      23 Livak KJ, "Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method" 25 : 402-408, 2001

      24 Hayama S., "Activation of CDCA1-KNTC2, members of centromere protein complex" 66 : 10339-10348, 2006

      25 Schneider J., "Abnormal oxidative metabolism of estradiol in women with breast cancer" 79 : 3047-3051, 1982

      26 McGuire WL, "A physiological role for estrogen and progesterone in breast cancer" 7 : 875-882, 1976

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2010-01-01 등재 등재학술지 유지 (등재유지) KCI등재
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      2007-05-09 학술지명변경 한글명 : Agricultrual Chemistry and Biotechnology -> Journal of Applied Biological Chemistry
      외국어명 : 미등록 -> Journal of Applied Biological Chemistry
      KCI등재
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      2003-01-01 등재 등재학술지 선정 (등재후보2차) KCI등재
      2002-01-01 등재 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2000-07-01 등재 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.41 0.41 0.39
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.4 0.44 0.741 0.16
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