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Updated: Jul 18, 2026

Establishing 3D Endometrial Organoids from the Mouse Uterus
Published on: January 6, 2023
Expression of organic cation transporter SLC22A16 in human endometria
Naoko Sato1, Kiyoshi Ito, Toru Onogawa
1Department of Obstetrics and Gynecology, Tohoku University Graduate School of Medicine, Sendai, Japan.
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.
Insights
The organic cation transporter SLC22A16 is highly expressed in the secretory phase of the endometrium. Its expression may be progesterone-regulated, suggesting potential use of progestins to enhance adriamycin chemotherapy for endometrial cancer.
Area of Science:
- Molecular biology
- Gynecologic oncology
- Pharmacology
Background:
- SLC22A16 is an organic cation transporter involved in adriamycin uptake.
- Adriamycin is a critical chemotherapeutic agent for endometrial cancer.
- Understanding SLC22A16 expression is crucial for optimizing endometrial cancer treatment.
Purpose of the Study:
- To investigate the expression of SLC22A16 in normal and cancerous human endometrium.
- To determine the regulation of SLC22A16 by progesterone.
- To explore the therapeutic implications of SLC22A16 expression in endometrial cancer.
Main Methods:
- Immunohistochemical analysis of SLC22A16 protein expression.
- Quantitative reverse transcription-polymerase chain reaction for mRNA levels.
- Assessment of SLC22A16 expression in endometrial tissues and cell lines, including response to progesterone.
Main Results:
- SLC22A16 protein expression is significantly higher in the secretory phase compared to the proliferative phase of normal endometrium.
- SLC22A16 protein and mRNA were detected in a subset of endometrial cancer specimens and cell lines.
- Progesterone exposure increased SLC22A16 mRNA levels in endometrial cancer cell lines.
Conclusions:
- SLC22A16 is expressed in human endometrium and its expression is modulated by the menstrual cycle phase and progesterone.
- SLC22A16 expression in endometrial cancer may influence response to adriamycin.
- Progestin therapy could potentially enhance adriamycin efficacy in endometrial cancers expressing SLC22A16.
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