{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T14:46:26Z","timestamp":1787064386920,"version":"build-2736575974"},"reference-count":34,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","license":[{"start":{"date-parts":[[2025,9,22]],"date-time":"2025-09-22T00:00:00Z","timestamp":1758499200000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100004480","name":"Natural Science Foundation of Shanxi Province","doi-asserted-by":"crossref","award":["202203021222356"],"award-info":[{"award-number":["202203021222356"]}],"id":[{"id":"10.13039\/501100004480","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/501100004480","name":"Natural Science Foundation of Shanxi Province","doi-asserted-by":"crossref","award":["202203021222356"],"award-info":[{"award-number":["202203021222356"]}],"id":[{"id":"10.13039\/501100004480","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["Kidney360"],"published-print":{"date-parts":[[2026,1]]},"abstract":"<jats:sec>\n                    <jats:title>Key Points<\/jats:title>\n                    <jats:p>\n                      <jats:list list-type=\"bullet\">\n                        <jats:list-item>\n                          <jats:p>\n                            In this study, we explored the role and mechanisms underlying the Wnt\/\n                            <jats:italic toggle=\"yes\">\u03b2<\/jats:italic>\n                            -catenin signaling pathway in the development of renal interstitial fibrosis\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Saracatinib effectively inhibits this pathway by binding to Fyn in kidney tissues, blocking the phosphorylation of\n                            <jats:italic toggle=\"yes\">\u03b2<\/jats:italic>\n                            -catenin at tyrosine 142.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>These findings suggest that saracatinib may offer a promising new therapeutic strategy for CKD treatment.<\/jats:p>\n                        <\/jats:list-item>\n                      <\/jats:list>\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Renal interstitial fibrosis is a common pathologic feature of CKD and is a critical determinant of disease progression. Recent studies have highlighted the significant role of the Wnt\/\n                      <jats:italic toggle=\"yes\">\u03b2<\/jats:italic>\n                      -catenin signaling pathway in the development of renal interstitial fibrosis, but the exact mechanisms remain unclear.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      Renal tissue samples from CKD patients with renal interstitial fibrosis who underwent renal biopsy at our center between January 2022 and December 2023 were selected for staining. In addition, a rat model of renal interstitial fibrosis was established using unilateral ureteral obstruction (UUO). UUO rats were administered low and high doses of saracatinib\n                      <jats:italic toggle=\"yes\">via<\/jats:italic>\n                      gavage for 2 weeks, followed by examination of changes in relevant indicators.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      In this study, we showed that in the kidney tissues of both CKD patients and rats with renal interstitial fibrosis, there was a marked upregulation of the tyrosine 142 kinase Fyn, which accompanied the excessive activation of the Wnt\/\n                      <jats:italic toggle=\"yes\">\u03b2<\/jats:italic>\n                      -catenin pathway. Saracatinib was found to inhibit this pathway by binding to Fyn in kidney tissues, thereby blocking the phosphorylation of\n                      <jats:italic toggle=\"yes\">\u03b2<\/jats:italic>\n                      -catenin at tyrosine 142. This inhibition (\n                      <jats:italic toggle=\"yes\">1<\/jats:italic>\n                      ) decreased the serum urea nitrogen and cystatin C levels, along with an increase in serum albumin and total protein concentration, and (\n                      <jats:italic toggle=\"yes\">2<\/jats:italic>\n                      ) alleviated renal interstitial fibrosis in the UUO rat model, resulting in an amelioration of the progression of renal interstitial fibrosis.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>This study suggests that saracatinib may be a novel therapeutic strategy for CKD treatment.<\/jats:p>\n                  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