Identification of SPRYD4 as a tumour suppressor predicts prognosis and correlates with immune infiltration in cholangiocarcinoma
© 2023. The Author(s)..
Cholangiocarcinoma (CCA) is an aggressive solid tumour with a 5-year survival rate ranging from 7% to 20%. It is, therefore, urgent to identify novel biomarkers and therapeutic targets to improve the outcomes of patients with CCA. SPRY-domain containing protein 4 (SPRYD4) contains SPRY domains that modulate protein-protein interaction in various biological processes; however, its role in cancer development is insufficiently explored. This study is the first to identify that SPRYD4 is downregulated in CCA tissues using multiple public datasets and a CCA cohort. Furthermore, the low expression of SPRYD4 was significantly associated with unfavourable clinicopathological characteristics and poor prognosis in patients with CCA, indicating that SPRYD4 could be a prognosis indicator of CCA. In vitro experiments revealed that SPRYD4 overexpression inhibited CCA cells proliferation and migration, whereas the proliferative and migratory capacity of CCA cells was enhanced after SPRYD4 deletion. Moreover, flow cytometry showed that SPRYD4 overexpression triggered the S/G2 cell phase arrest and promoted apoptosis in CCA cells. Furthermore, the tumour-inhibitory effect of SPRYD4 was validated in vivo using xenograft mouse models. SPRYD4 also showed a close association with tumour-infiltrating lymphocytes and important immune checkpoints including PD1, PD-L1 and CTLA4 in CCA. In conclusion, this study elucidated the role of SPRYD4 during CCA development and highlighted SPRYD4 as a novel biomarker and tumour suppressor in CCA.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:23 |
---|---|
Enthalten in: |
BMC cancer - 23(2023), 1 vom: 04. Mai, Seite 404 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Ma, Zuyi [VerfasserIn] |
---|
Links: |
---|
Themen: |
Cholangiocarcinoma |
---|
Anmerkungen: |
Date Completed 08.05.2023 Date Revised 08.05.2023 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.1186/s12885-023-10810-9 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM356462412 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM356462412 | ||
003 | DE-627 | ||
005 | 20231226070520.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1186/s12885-023-10810-9 |2 doi | |
028 | 5 | 2 | |a pubmed24n1188.xml |
035 | |a (DE-627)NLM356462412 | ||
035 | |a (NLM)37142983 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Ma, Zuyi |e verfasserin |4 aut | |
245 | 1 | 0 | |a Identification of SPRYD4 as a tumour suppressor predicts prognosis and correlates with immune infiltration in cholangiocarcinoma |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 08.05.2023 | ||
500 | |a Date Revised 08.05.2023 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023. The Author(s). | ||
520 | |a Cholangiocarcinoma (CCA) is an aggressive solid tumour with a 5-year survival rate ranging from 7% to 20%. It is, therefore, urgent to identify novel biomarkers and therapeutic targets to improve the outcomes of patients with CCA. SPRY-domain containing protein 4 (SPRYD4) contains SPRY domains that modulate protein-protein interaction in various biological processes; however, its role in cancer development is insufficiently explored. This study is the first to identify that SPRYD4 is downregulated in CCA tissues using multiple public datasets and a CCA cohort. Furthermore, the low expression of SPRYD4 was significantly associated with unfavourable clinicopathological characteristics and poor prognosis in patients with CCA, indicating that SPRYD4 could be a prognosis indicator of CCA. In vitro experiments revealed that SPRYD4 overexpression inhibited CCA cells proliferation and migration, whereas the proliferative and migratory capacity of CCA cells was enhanced after SPRYD4 deletion. Moreover, flow cytometry showed that SPRYD4 overexpression triggered the S/G2 cell phase arrest and promoted apoptosis in CCA cells. Furthermore, the tumour-inhibitory effect of SPRYD4 was validated in vivo using xenograft mouse models. SPRYD4 also showed a close association with tumour-infiltrating lymphocytes and important immune checkpoints including PD1, PD-L1 and CTLA4 in CCA. In conclusion, this study elucidated the role of SPRYD4 during CCA development and highlighted SPRYD4 as a novel biomarker and tumour suppressor in CCA | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Cholangiocarcinoma | |
650 | 4 | |a Prognosis | |
650 | 4 | |a SPRYD4 | |
650 | 4 | |a Tumor immune infiltration | |
650 | 4 | |a Tumor suppressor | |
650 | 7 | |a SPRYD4 protein, human |2 NLM | |
650 | 7 | |a Nuclear Proteins |2 NLM | |
700 | 1 | |a Xie, Tiange |e verfasserin |4 aut | |
700 | 1 | |a Sun, Jia |e verfasserin |4 aut | |
700 | 1 | |a Yu, Jianchun |e verfasserin |4 aut | |
700 | 1 | |a Huang, Shanzhou |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Qi |e verfasserin |4 aut | |
700 | 1 | |a Li, Binglu |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t BMC cancer |d 2001 |g 23(2023), 1 vom: 04. Mai, Seite 404 |w (DE-627)NLM111431948 |x 1471-2407 |7 nnns |
773 | 1 | 8 | |g volume:23 |g year:2023 |g number:1 |g day:04 |g month:05 |g pages:404 |
856 | 4 | 0 | |u http://dx.doi.org/10.1186/s12885-023-10810-9 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 23 |j 2023 |e 1 |b 04 |c 05 |h 404 |