Literature DB >> 17197897

Expression of organic cation transporter SLC22A16 in human endometria.

Naoko Sato1, Kiyoshi Ito, Toru Onogawa, Jun-Ichi Akahira, Michiaki Unno, Takaaki Abe, Hitoshi Niikura, Nobuo Yaegashi.   

Abstract

SLC22A16 is one of newly isolated organic cation transporters, which is responsible for uptake and transport of adriamycin into cells. Adriamycin is one of the key drugs for treatment of endometrial cancer. Therefore, we examined expression of SLC22A16 in human endometrium and its disorders. Protein and mRNA expression levels of SLC22A16 were examined in 124 endometrial cancer specimens, 25 normal endometrial tissue samples (15 in proliferative phase, 10 in secretory phase), and 7 endometrial cancer cell lines using immunohistochemical analysis and reverse transcription-polymerase chain reaction. Changes in SLC22A16 mRNA expression level after progesterone exposure were also examined. Immunohistochemical analysis showed that SLC22A16 protein was highly expressed in endometrium during the normal secretory phase, but its level was significantly reduced in the proliferative phase. SLC22A16 protein was detected in 59 of 124 (48%) endometrial cancer specimens and 3 of 7 (43%) endometrial cancer cell lines. The mRNA levels measured by quantitative reverse transcription-polymerase chain reaction were comparable with levels of protein expression. Furthermore, SLC22A16 mRNA levels were increased in endometrial cancer cell lines in the presence of progesterone. In conclusion, SLC22A16 is expressed in various endometrial tissues. Its expression level is high during the secretory phase and may be regulated by progesterone. Our findings also suggest that it may be possible to use progestins to increase the response of endometrioid endometrial carcinoma with SLC22A16 expression to adriamycin-based chemotherapeutic regimens.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17197897     DOI: 10.1097/01.pgp.0000225845.67245.b3

Source DB:  PubMed          Journal:  Int J Gynecol Pathol        ISSN: 0277-1691            Impact factor:   2.762


  6 in total

1.  Cellular pharmacokinetic mechanisms of adriamycin resistance and its modulation by 20(S)-ginsenoside Rh2 in MCF-7/Adr cells.

Authors:  Jingwei Zhang; Fang Zhou; Xiaolan Wu; Xiaoxuan Zhang; Yuancheng Chen; Beth S Zha; Fang Niu; Meng Lu; Gang Hao; Yuan Sun; Jianguo Sun; Ying Peng; Guangji Wang
Journal:  Br J Pharmacol       Date:  2012-01       Impact factor: 8.739

2.  Bacterial over-expression of functionally active human CT2 (SLC22A16) carnitine transporter.

Authors:  Michele Galluccio; Tiziano Mazza; Mariafrancesca Scalise; Maria Chiara Sarubbi; Cesare Indiveri
Journal:  Mol Biol Rep       Date:  2022-05-24       Impact factor: 2.742

3.  Route-specific association of progestin therapy and concurrent metformin use in obese women with complex atypical hyperplasia.

Authors:  Koji Matsuo; Rachel S Mandelbaum; Marcia Ciccone; Mahdi Khoshchehreh; Heena Pursuwani; Elise B Morocco; Shinya Matsuzaki; Christina E Dancz; Begum Ozel; Richard J Paulson; Lynda Roman
Journal:  Int J Gynecol Cancer       Date:  2020-05-05       Impact factor: 3.437

4.  The human carnitine transporter SLC22A16 mediates high affinity uptake of the anticancer polyamine analogue bleomycin-A5.

Authors:  Mustapha Aouida; Richard Poulin; Dindial Ramotar
Journal:  J Biol Chem       Date:  2009-12-25       Impact factor: 5.157

5.  The human organic cation transporter OCT1 mediates high affinity uptake of the anticancer drug daunorubicin.

Authors:  Emil Andreev; Nicolas Brosseau; Euridice Carmona; Anne-Marie Mes-Masson; Dindial Ramotar
Journal:  Sci Rep       Date:  2016-02-10       Impact factor: 4.379

Review 6.  Organic Cation Transporters in Human Physiology, Pharmacology, and Toxicology.

Authors:  Sophia L Samodelov; Gerd A Kullak-Ublick; Zhibo Gai; Michele Visentin
Journal:  Int J Mol Sci       Date:  2020-10-24       Impact factor: 5.923

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.