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We are analyzing https://link.springer.com/article/10.1007/s43032-021-00531-4.

Title:
Aberrant Expression of Sodium-Potassium-Chloride Cotransporter in Endometriosis | Reproductive Sciences
Description:
Cell membrane ion channels have important roles in cell migration during cancer development and metastasis. Although endometriosis is a benign gynecological disease, some migration and invasion characteristics of endometriosis are similar to those of cancer. However, only a few studies have examined cell membrane ion channels and their associations with endometriosis. This study aimed to investigate the effects of these ion channels on development of endometriosis. A total of 39 women who underwent laparoscopic ovarian cyst enucleation were included in the study population. Eutopic endometrium or ectopic endometrium tissues were obtained from each patient based on allocation to an endometriosis group (n=21) or a control group (n=18). Quantitative real-time PCR (qRT-PCR) and western blot analyses were performed to quantify NKCC1, NKCC2, and CLCN3 mRNA expression and protein concentrations. SiRNA transfection and migration assays of the endometrial stromal cells were performed to test the effects of the ion channels on the migration ability. The qRT-PCR and western blot analyses revealed significantly elevated mRNA expression and protein expression of NKCC1, NKCC2, and CLCN3 in the ectopic endometrial tissue from the patients with endometriosis (p < 0.05). Migration assay of siRNA transfected cells suggested a decreased migratory potential of the endometrial stromal cells (p < 0.001). The magnitudes of expression of NKCC1, NKCC2, and CLCN3 were positively correlated with endometrioma size. The increased expression of NKCC1, NKCC2, and CLCN3 in endometriosis offers opportunities to understand mechanisms of endometriosis and develop novel therapeutic approaches.
Website Age:
28 years and 1 months (reg. 1997-05-29).

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {🔍}

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Topics {✒️}

young sik choi sodium-potassium-chloride cotransporter month download article/chapter myung jae jeon chloride channel-3 endometrial stem/progenitor cells affecting g0/g1 state western blot analyses regulating mir-15a-5p quantitative real-time pcr byung seok lee mutation profiles tumour cell migration comprehensive array-based analysis targeting ion channels author information authors egfr-mutated adenocarcinoma patients ectopic endometrial cells jae hoon lee pancreatic epithelial cells endometrial stromal cells endometrial cancer proliferation sihyun cho revised cell volume regulation ectopic endometrial tissue privacy choices/manage cookies related subjects author correspondence full article pdf joo hyun park cell migration seok kyo seo ion channels clcn3 mrna expression made substantial contributions jeong sook kim korea health technology check access instant access ji hyun park code availability aberrant expression puerarin suppresses invasion protein expression original article published european economic area bo hee won bo hyon yun benign gynecological disease author

Schema {🗺️}

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         headline:Aberrant Expression of Sodium-Potassium-Chloride Cotransporter in Endometriosis
         description:Cell membrane ion channels have important roles in cell migration during cancer development and metastasis. Although endometriosis is a benign gynecological disease, some migration and invasion characteristics of endometriosis are similar to those of cancer. However, only a few studies have examined cell membrane ion channels and their associations with endometriosis. This study aimed to investigate the effects of these ion channels on development of endometriosis. A total of 39 women who underwent laparoscopic ovarian cyst enucleation were included in the study population. Eutopic endometrium or ectopic endometrium tissues were obtained from each patient based on allocation to an endometriosis group (n=21) or a control group (n=18). Quantitative real-time PCR (qRT-PCR) and western blot analyses were performed to quantify NKCC1, NKCC2, and CLCN3 mRNA expression and protein concentrations. SiRNA transfection and migration assays of the endometrial stromal cells were performed to test the effects of the ion channels on the migration ability. The qRT-PCR and western blot analyses revealed significantly elevated mRNA expression and protein expression of NKCC1, NKCC2, and CLCN3 in the ectopic endometrial tissue from the patients with endometriosis (p < 0.05). Migration assay of siRNA transfected cells suggested a decreased migratory potential of the endometrial stromal cells (p < 0.001). The magnitudes of expression of NKCC1, NKCC2, and CLCN3 were positively correlated with endometrioma size. The increased expression of NKCC1, NKCC2, and CLCN3 in endometriosis offers opportunities to understand mechanisms of endometriosis and develop novel therapeutic approaches.
         datePublished:2021-03-11T00:00:00Z
         dateModified:2021-03-24T00:00:00Z
         pageStart:2641
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            Endometriosis
            NKCC
            Membrane channel
            Cell migration
            Reproductive Medicine
            Embryology
            Obstetrics/Perinatology/Midwifery
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      headline:Aberrant Expression of Sodium-Potassium-Chloride Cotransporter in Endometriosis
      description:Cell membrane ion channels have important roles in cell migration during cancer development and metastasis. Although endometriosis is a benign gynecological disease, some migration and invasion characteristics of endometriosis are similar to those of cancer. However, only a few studies have examined cell membrane ion channels and their associations with endometriosis. This study aimed to investigate the effects of these ion channels on development of endometriosis. A total of 39 women who underwent laparoscopic ovarian cyst enucleation were included in the study population. Eutopic endometrium or ectopic endometrium tissues were obtained from each patient based on allocation to an endometriosis group (n=21) or a control group (n=18). Quantitative real-time PCR (qRT-PCR) and western blot analyses were performed to quantify NKCC1, NKCC2, and CLCN3 mRNA expression and protein concentrations. SiRNA transfection and migration assays of the endometrial stromal cells were performed to test the effects of the ion channels on the migration ability. The qRT-PCR and western blot analyses revealed significantly elevated mRNA expression and protein expression of NKCC1, NKCC2, and CLCN3 in the ectopic endometrial tissue from the patients with endometriosis (p < 0.05). Migration assay of siRNA transfected cells suggested a decreased migratory potential of the endometrial stromal cells (p < 0.001). The magnitudes of expression of NKCC1, NKCC2, and CLCN3 were positively correlated with endometrioma size. The increased expression of NKCC1, NKCC2, and CLCN3 in endometriosis offers opportunities to understand mechanisms of endometriosis and develop novel therapeutic approaches.
      datePublished:2021-03-11T00:00:00Z
      dateModified:2021-03-24T00:00:00Z
      pageStart:2641
      pageEnd:2648
      sameAs:https://doi.org/10.1007/s43032-021-00531-4
      keywords:
         Endometriosis
         NKCC
         Membrane channel
         Cell migration
         Reproductive Medicine
         Embryology
         Obstetrics/Perinatology/Midwifery
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            1933-7205
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         type:
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         name:Springer International Publishing
         logo:
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            type:ImageObject
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      author:
            name:Inha Lee
            affiliation:
                  name:Yonsei University College of Medicine
                  address:
                     name:Department of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea
                     type:PostalAddress
                  type:Organization
                  name:Yonsei University College of Medicine
                  address:
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                  address:
                     name:Department of Obstetrics and Gynecology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, South Korea
                     type:PostalAddress
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            name:Jeong Sook Kim
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                  name:University of Ulsan College of Medicine, Ulsan University Hospital
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                     name:Department of Obstetrics and Gynecology, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, South Korea
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                  name:Gangnam Severance Hospital, Yonsei University College of Medicine
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            name:Bo Hee Won
            affiliation:
                  name:Yonsei University College of Medicine
                  address:
                     name:Institute of Women’s Life Medical Science, Yonsei University College of Medicine, Seoul, South Korea
                     type:PostalAddress
                  type:Organization
                  name:Gangnam Severance Hospital, Yonsei University College of Medicine
                  address:
                     name:Department of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Gangnam-gu, South Korea
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Heeyon Kim
            affiliation:
                  name:Yonsei University College of Medicine
                  address:
                     name:Department of Obstetrics and Gynecology, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea
                     type:PostalAddress
                  type:Organization
                  name:Yonsei University College of Medicine
                  address:
                     name:Institute of Women’s Life Medical Science, Yonsei University College of Medicine, Seoul, South Korea
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jae Hoon Lee
            affiliation:
                  name:Yonsei University College of Medicine
                  address:
                     name:Institute of Women’s Life Medical Science, Yonsei University College of Medicine, Seoul, South Korea
                     type:PostalAddress
                  type:Organization
                  name:Gangnam Severance Hospital, Yonsei University College of Medicine
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                     type:PostalAddress
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                  name:Yonsei University College of Medicine
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