PANcreatic-DERived factor: Novel hormone PANDERing to glucose regulation
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| Title: | PANcreatic-DERived factor: Novel hormone PANDERing to glucose regulation |
|---|---|
| Authors: | Wilson, Camella G.1, Robert-Cooperman, Claudia E.2, Burkhardt, Brant R.2,3 bburkhardt@usf.edu |
| Source: | FEBS Letters. Jul2011, Vol. 585 Issue 14, p2137-2143. 7p. |
| Subjects: | Islands of Langerhans, Cytokines, Glucose, Gene expression, Apoptosis, Treatment of diabetes, Animal models in research |
| Abstract: | Abstract: PANcreatic-DERived factor (PANDER, FAM3B) is a member of the FAM3 family of cytokine molecules that were initially described in 2002. PANDER expression is primarily localized to the endocrine pancreas and is secreted from both pancreatic α and β-cells. Initial characterization of PANDER revealed a potential role in pancreatic islet apoptosis. However, recent animal models have indicated PANDER functions as a hormone by regulating glucose levels via interaction with both the liver and the endocrine pancreas. An understanding of the function of PANDER can further the insight into the mechanisms of glucose regulation and potentially provide additional therapeutic targets for the treatment of diabetes. This review details the supporting data demonstrating PANDER has a biological function in glycemic regulation. [Copyright &y& Elsevier] |
| Copyright of FEBS Letters is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 62976648 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: PANcreatic-DERived factor: Novel hormone PANDERing to glucose regulation – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wilson%2C+Camella+G%2E%22">Wilson, Camella G.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Robert-Cooperman%2C+Claudia+E%2E%22">Robert-Cooperman, Claudia E.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Burkhardt%2C+Brant+R%2E%22">Burkhardt, Brant R.</searchLink><relatesTo>2,3</relatesTo><i> bburkhardt@usf.edu</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22FEBS+Letters%22">FEBS Letters</searchLink>. Jul2011, Vol. 585 Issue 14, p2137-2143. 7p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Islands+of+Langerhans%22">Islands of Langerhans</searchLink><br /><searchLink fieldCode="DE" term="%22Cytokines%22">Cytokines</searchLink><br /><searchLink fieldCode="DE" term="%22Glucose%22">Glucose</searchLink><br /><searchLink fieldCode="DE" term="%22Gene+expression%22">Gene expression</searchLink><br /><searchLink fieldCode="DE" term="%22Apoptosis%22">Apoptosis</searchLink><br /><searchLink fieldCode="DE" term="%22Treatment+of+diabetes%22">Treatment of diabetes</searchLink><br /><searchLink fieldCode="DE" term="%22Animal+models+in+research%22">Animal models in research</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Abstract: PANcreatic-DERived factor (PANDER, FAM3B) is a member of the FAM3 family of cytokine molecules that were initially described in 2002. PANDER expression is primarily localized to the endocrine pancreas and is secreted from both pancreatic α and β-cells. Initial characterization of PANDER revealed a potential role in pancreatic islet apoptosis. However, recent animal models have indicated PANDER functions as a hormone by regulating glucose levels via interaction with both the liver and the endocrine pancreas. An understanding of the function of PANDER can further the insight into the mechanisms of glucose regulation and potentially provide additional therapeutic targets for the treatment of diabetes. This review details the supporting data demonstrating PANDER has a biological function in glycemic regulation. [Copyright &y& Elsevier] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of FEBS Letters is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.febslet.2011.05.059 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 2137 Subjects: – SubjectFull: Islands of Langerhans Type: general – SubjectFull: Cytokines Type: general – SubjectFull: Glucose Type: general – SubjectFull: Gene expression Type: general – SubjectFull: Apoptosis Type: general – SubjectFull: Treatment of diabetes Type: general – SubjectFull: Animal models in research Type: general Titles: – TitleFull: PANcreatic-DERived factor: Novel hormone PANDERing to glucose regulation Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wilson, Camella G. – PersonEntity: Name: NameFull: Robert-Cooperman, Claudia E. – PersonEntity: Name: NameFull: Burkhardt, Brant R. IsPartOfRelationships: – BibEntity: Dates: – D: 21 M: 07 Text: Jul2011 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 00145793 Numbering: – Type: volume Value: 585 – Type: issue Value: 14 Titles: – TitleFull: FEBS Letters Type: main |
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