The role of canopy family proteins: biological mechanism and disease function

被引:0
作者
Li, Xue [1 ]
Yin, Min-Yue [1 ]
Zhang, Shu-Tian [1 ,2 ]
Xie, Si-An [1 ,2 ]
机构
[1] Capital Med Univ, Beijing Friendship Hosp, Dept Gastroenterol, 95 Yong Rd, Beijing 100050, Peoples R China
[2] Beijing Digest Dis Ctr, Natl Clin Res Ctr Digest Dis, State Key Lab Digest Hlth, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
CNPY2; CNPY3; Unfolded protein response; Angiogenesis; Cancer; TOLL-LIKE-RECEPTOR; EXPRESSION; CNPY2; CELLS; ACTIVATION; REGULATOR; PATHWAY; GROWTH; PRAT4A; PROLIFERATION;
D O I
10.1007/s11033-025-10269-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Canopy family proteins are highly sequence-conserved proteins with an N-terminal hydrophobic signal sequence, a unique pattern of six cysteine residues characteristic of the saposin-like proteins, and a C-terminal putative endoplasmic reticulum retention signal sequence. At present, the known canopy family proteins are canopy fibroblast growth factor signaling regulator 1 (CNPY1), CNPY2, CNPY3, and CNPY4. Despite similar structures, canopy family proteins regulate complex signal networks to participate in various biological processes. They are involved in a wide range of diseases, including angiogenesis, abnormal immune responses, neurodevelopmental disorders, and the development of tumors. Here, we summarized the biological processes and influence on the disease of every CNPY family protein to elucidate potential biomarkers and point out the direction for future in-depth research.
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页数:11
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共 60 条
[1]   MSAP is a novel MIR-interacting protein that enhances neurite outgrowth and increases myosin regulatory light chain [J].
Bornhauser, BC ;
Olsson, PA ;
Lindholm, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) :35412-35420
[2]   A short guided tour through functional and structural features of saposin-like proteins [J].
Bruhn, H .
BIOCHEMICAL JOURNAL, 2005, 389 :249-257
[3]   Autism Associated Gene, ENGRAILED2, and Flanking Gene Levels Are Altered in Post-Mortem Cerebellum [J].
Choi, Jiyeon ;
Ababon, Myka R. ;
Soliman, Mai ;
Lin, Yong ;
Brzustowicz, Linda M. ;
Matteson, Paul G. ;
Millonig, James H. .
PLOS ONE, 2014, 9 (02)
[4]   Protective effect of Barbaloin in a rat model of myocardial ischemia reperfusion injury through the regulation of the CNPY2-PERK pathway [J].
Cui, Yue ;
Wang, Yongqiang ;
Liu, Gang .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2019, 43 (05) :2015-2023
[5]   Gene co-expression network analysis identifies the hub genes associated with immune functions for nocturnal hemodialysis in patients with end-stage renal disease [J].
Dai, Hongwei ;
Zhou, Jiao ;
Zhu, Bo .
MEDICINE, 2018, 97 (37)
[6]   Endometrial stromal cell proteome mapping in repeated implantation failure and recurrent pregnancy loss cases and fertile women [J].
Dhaenens, Lien ;
Lierman, Sylvie ;
De Clerck, Laura ;
Govaert, Elisabeth ;
Deforce, Dieter ;
Tilleman, Kelly ;
De Sutter, Petra .
REPRODUCTIVE BIOMEDICINE ONLINE, 2019, 38 (03) :442-454
[7]   CNPY2 enhances resistance to apoptosis induced by cisplatin via activation of NF-κB pathway in human non-small cell lung cancer [J].
Dou, Yu ;
Yu, Qin ;
Lei, Jun-qiang ;
Guo, Shun-lin .
BIOMEDICINE & PHARMACOTHERAPY, 2018, 103 :1658-1663
[8]   The CNPY2 enhances epithelial-mesenchymal transition via activating the AKT/GSK3 pathway in non-small cell lung cancer [J].
Dou, Yu ;
Lei, Jun-Qiang ;
Guo, Shun-Lin ;
Zhao, Da ;
Yue, Hong-Mei ;
Yu, Qin .
CELL BIOLOGY INTERNATIONAL, 2018, 42 (08) :959-964
[9]   Epigenetics of Genes Preferentially Expressed in Dissimilar Cell Populations: Myoblasts and Cerebellum [J].
Ehrlich, Melanie ;
Ehrlich, Kenneth C. ;
Lacey, Michelle ;
Baribault, Carl ;
Sen, Sagnik ;
Esteve, Pierre-Olivier ;
Pradhan, Sriharsa .
EPIGENOMES, 2024, 8 (01)
[10]   A protein interaction network centered on leucine-rich repeats and immunoglobulin-like domains 1 (LRIG1) regulates growth factor receptors [J].
Faraz, Mahmood ;
Herdenberg, Carl ;
Holmlund, Camilla ;
Henriksson, Roger ;
Hedman, Hakan .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (09) :3421-3435