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editDescriptionCancers-13-02968-g001-550.jpg |
English: Figure 1. (A) Mechanism of action of FGFR inhibitors and FGFR signaling pathway: FGFR inhibitors act by inhibiting the FGFR downstream signaling pathway (B) Pathophysiology of FGFR-inhibitor-associated hyperphosphatemia: In kidneys, FGFR inhibitors _target FGF23 ligand and FGFR1 receptor complex in the presence of klotho. Activation of the FGF23-FGFR1 pathway leads to inhibition of 25-OH vitamin D activation and degradation of 1, 25 (OH)2 vitamin D. FGFR inhibitors block the catabolism of 1, 25 (OH)2 vitamin D, and sodium-phosphate co-transporters in the proximal renal tubule cell thereby leading to hyperphosphatemia. (C) Pathophysiology of FGFR inhibitor-associated diarrhea: The FGFR4/FGF19/ERK1/2 pathway potentiates the conversion of cholesterol to bile acid in the liver. FGFR inhibitors block the conversion of cholesterol to bile acid thereby leading to altered bile acid metabolism. |
Date | |
Source | https://www.mdpi.com/2072-6694/13/12/2968 |
Author | Kommalapati, A.; Tella, S.H.; Borad, M.; Javle, M.; Mahipal, A. |
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current | 12:48, 19 June 2024 | 499 × 389 (110 KB) | Doc James (talk | contribs) | Cropped 9 % horizontally, 10 % vertically, 19 % areawise using CropTool with precise mode. | |
23:01, 16 June 2024 | 550 × 434 (94 KB) | Ozzie10aaaa (talk | contribs) | Uploaded a work by Kommalapati, A.; Tella, S.H.; Borad, M.; Javle, M.; Mahipal, A. from https://www.mdpi.com/2072-6694/13/12/2968 with UploadWizard |
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