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- Publisher Website: 10.3390/cancers13143588
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Article: Repurposing DPP-4 inhibitors for colorectal cancer: A retrospective and single center study
Title | Repurposing DPP-4 inhibitors for colorectal cancer: A retrospective and single center study |
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Authors | |
Keywords | colorectal cancer DPP4 CD26 DPP4-inhibitor gliptin |
Issue Date | 2021 |
Publisher | MDPI AG. The Journal's web site is located at http://www.mdpi.com/journal/cancers/ |
Citation | Cancers, 2021, v. 13 n. 14, p. article no. 3588 How to Cite? |
Abstract | Background: There have been studies reporting the crucial roles of Dipeptidyl-peptidase 4 (DPP4) in colorectal cancer (CRC) initiation and progression, whereas DPP4-inhibitors are safe Food and Drug Association (FDA)-approved drugs for treating diabetes. This study aims to investigate the association between DPP4-inhibitor treatment and the prognosis of CRC patients. Methods: Clinical data of CRC patients with diabetes and the prescription of DPP4-inhibitors who had undergone curative surgery in our hospital between January 2006 and December 2015 were retrieved. Their survival data and immune cell population in circulatory blood were compared to those treated with metformin. Results: The DPP4-inhibitor patient group showed a significantly better 5-year disease-free survival (median DFS = 1733 days, 95% CI = 1596 to 1870 days) when compared to the metformin group (p = 0.030, median DFS = 1382 days, 95% CI = 1246 to 1518 days). 33 out of the 92 patients in the metformin group showed recurrence whereas only 3 of the 26 patients in the DPP4-inhibitor group showed recurrence (p = 0.033). Cox regression analysis demonstrated that DPP4-inhibitor application is a favorable factor associated with a lower risk of recurrence (Hazard ratio = 0.200, p = 0.035). Furthermore, our results suggested that the immune cell profile of CRC patients is a potential biomarker for response to DPP4-inhibitor treatment. Conclusion: This study demonstrated the association of DPP4-inhibitor treatment with a better prognosis of CRC patients. |
Persistent Identifier | http://hdl.handle.net/10722/301660 |
ISSN | 2023 Impact Factor: 4.5 2023 SCImago Journal Rankings: 1.391 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ng, L | - |
dc.contributor.author | Foo, DCC | - |
dc.contributor.author | Wong, CKH | - |
dc.contributor.author | Man, ATK | - |
dc.contributor.author | Lo, OSH | - |
dc.contributor.author | Law, WL | - |
dc.date.accessioned | 2021-08-09T03:42:21Z | - |
dc.date.available | 2021-08-09T03:42:21Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Cancers, 2021, v. 13 n. 14, p. article no. 3588 | - |
dc.identifier.issn | 2072-6694 | - |
dc.identifier.uri | http://hdl.handle.net/10722/301660 | - |
dc.description.abstract | Background: There have been studies reporting the crucial roles of Dipeptidyl-peptidase 4 (DPP4) in colorectal cancer (CRC) initiation and progression, whereas DPP4-inhibitors are safe Food and Drug Association (FDA)-approved drugs for treating diabetes. This study aims to investigate the association between DPP4-inhibitor treatment and the prognosis of CRC patients. Methods: Clinical data of CRC patients with diabetes and the prescription of DPP4-inhibitors who had undergone curative surgery in our hospital between January 2006 and December 2015 were retrieved. Their survival data and immune cell population in circulatory blood were compared to those treated with metformin. Results: The DPP4-inhibitor patient group showed a significantly better 5-year disease-free survival (median DFS = 1733 days, 95% CI = 1596 to 1870 days) when compared to the metformin group (p = 0.030, median DFS = 1382 days, 95% CI = 1246 to 1518 days). 33 out of the 92 patients in the metformin group showed recurrence whereas only 3 of the 26 patients in the DPP4-inhibitor group showed recurrence (p = 0.033). Cox regression analysis demonstrated that DPP4-inhibitor application is a favorable factor associated with a lower risk of recurrence (Hazard ratio = 0.200, p = 0.035). Furthermore, our results suggested that the immune cell profile of CRC patients is a potential biomarker for response to DPP4-inhibitor treatment. Conclusion: This study demonstrated the association of DPP4-inhibitor treatment with a better prognosis of CRC patients. | - |
dc.language | eng | - |
dc.publisher | MDPI AG. The Journal's web site is located at http://www.mdpi.com/journal/cancers/ | - |
dc.relation.ispartof | Cancers | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | colorectal cancer | - |
dc.subject | DPP4 | - |
dc.subject | CD26 | - |
dc.subject | DPP4-inhibitor | - |
dc.subject | gliptin | - |
dc.title | Repurposing DPP-4 inhibitors for colorectal cancer: A retrospective and single center study | - |
dc.type | Article | - |
dc.identifier.email | Ng, L: luing@hku.hk | - |
dc.identifier.email | Foo, DCC: ccfoo@hku.hk | - |
dc.identifier.email | Wong, CKH: carlosho@hku.hk | - |
dc.identifier.email | Man, ATK: tkman@hku.hk | - |
dc.identifier.email | Lo, OSH: oswens@HKUCC-COM.hku.hk | - |
dc.identifier.email | Law, WL: lawwl@hkucc.hku.hk | - |
dc.identifier.authority | Ng, L=rp02207 | - |
dc.identifier.authority | Foo, DCC=rp01899 | - |
dc.identifier.authority | Wong, CKH=rp01931 | - |
dc.identifier.authority | Law, WL=rp00436 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.3390/cancers13143588 | - |
dc.identifier.pmid | 34298800 | - |
dc.identifier.pmcid | PMC8306906 | - |
dc.identifier.scopus | eid_2-s2.0-85110170657 | - |
dc.identifier.hkuros | 323964 | - |
dc.identifier.volume | 13 | - |
dc.identifier.issue | 14 | - |
dc.identifier.spage | article no. 3588 | - |
dc.identifier.epage | article no. 3588 | - |
dc.identifier.isi | WOS:000676705700001 | - |
dc.publisher.place | Switzerland | - |