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논문 기본 정보

자료유형
학술저널
저자정보
Kyu Youn Ahn (Chonnam National University Medical School) Pham Ngoc Khoi (Pham Ngoc Thach University of Medicine) Young Suk Cho (Chonnam National University Medical School) Shinan Li (Chonnam National University Medical School) Dhiraj Kumar Sah (Chonnam National University Medical School) Yong Xia (Jining Medical University) Young Do Jung (Chonnam National University Medical School)
저널정보
대한체질인류학회 해부·생물인류학 해부·생물인류학 제34권 제1호
발행연도
2021.3
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21 - 30 (10page)

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Intracellular adhesion molecule-1 (ICAM-1) belongs to the immunoglobulin-like superfamily of adhesion molecules that mediate cell adhesion to other cells, and ICAM-1 is involved in cancer progression and recurrence. Since the ICAM-1 is considered as one of the therapeutic target against bladder cancer, we examined whether sulforaphane, an aliphatic isothiocyanate, could inhibit ICAM-1 expression in bladder cancer T24 cells. Sulforaphane inhibited phorbol 12-myristate 13-acetate (PMA)-induced ICAM-1 expression at the mRNA and protein levels in human bladder cancer cells, as revealed by reverse transcriptase polymerase chain reaction and western blot analyses, respectively. Specific inhibitor studies have shown that the transcription factors, activator protein-1 (AP-1) and nuclear factor-kappa B (NF-κB), are involved in PMA-induced ICAM-1 expression. We found that sulforaphane inhibited the activation of both AP-1 and NF-κB induced by PMA in bladder cancer cells. Interestingly, we also found that sulforaphane abrogated PMA-induced THP-1 monocyte adhesion to bladder cancer cells. Collectively, our results provide experimental evidence that sulforaphane could serve as a new therapeutic candidate against bladder cancer.

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Abstract
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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