Publication for SPARC and FSTL1
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | SPARC | secreted protein acidic and cysteine rich | 6678 | [link] | ||
| hsa | FSTL1 | follistatin like 1 | 11167 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 27886258 | 0.98 | FSTL-1 staining was observed at the cell surface, all members of the SPARC family also demonstrated cytoplasmic staining, and in some cases staining in the nucleus could also be observed. |
| 0.97 | FSTL-1 is sometimes overlooked as a member of the SPARC family since it has the least structural and sequence homology to SPARC and it has been suggested that the calcium binding EF hand in FSTL-1 may be non-functional. | |
| 0.97 | FSTL-1 is expressed by stromal cells within the pancreas with an expression pattern highly reminiscent of SPARC, and is expressed at high levels specifically by pancreatic stellate cells. | |
| 0.97 | SPARC-like expression pattern, exogenous FSTL-1 does not regulate beta cell growth or proliferation | |
| 0.96 | FSTL-1 was the most highly specific of the SPARC family proteins. | |
| 0.96 | SPARC, FSTL-1 is therefore unlikely to be directly involved in the regulation of islet growth and survival. | |
| 0.94 | SPARC family proteins, with the exception of FSTL-1. | |
| 0.94 | FSTL-1 may play a related role to SPARC in pancreatic disease and that the function of FSTL-1 warrants further study. | |
| 0.94 | SPARC, FSTL-1 has been shown to regulate signalling of the TGF-beta superfamily and to regulate growth factor signalling. | |
| 0.93 | FSTL-1 expression is localised to the stromal compartment reminiscent of SPARC. | |
| 0.91 | FSTL-1 has the lowest homology to SPARC. | |
| 0.89 | FSTL-1 inhibits pancreatic cancer cell growth, suggesting that SPARC and FSTL-1 produced by stromal cells have antagonistic effects on cancer cell growth. | |
| 0.58 | SPARC family protein complexity reveals FSTL-1 as an inhibitor of pancreatic cancer cell growth | |
| 27626636 | 0.98 | SPARC family of proteins consists of SPARC (osteonectin), Hevin (SPARC-like protein 1), secreted modular calcium binding protein (SMOC) 1 and 2, testican-1, 2 and 3, and follistatin like protein 1. |
| 26199111 | 0.97 | FSTL1 or SPARC after GHRT (ESM 1: Fig. S4), which might require stimulation with an acute exercise bout. |
| 0.96 | SPARC levels after exercise suppressed colon tumorigenesis and muscle-derived FSTL1 attenuated neointimal formation in response to arterial injury. | |
| 0.90 | FSTL1 and SPARC are linked to inflammation and insulin resistance. | |
| 29435136 | 0.97 | SPARC, FSTL1 was recently shown to inhibit pancreatic cancer growth. |
| 0.95 | SPARC (secreted protein acidic and rich in cysteine) family of matricellular proteins, which has 8 members: SPARC, SPARCL1/Hevin, SPOCK1, -2, -3, SMOC1, -2 and FSTL1. | |
| 24090399 | 0.97 | FSTL1, CHI3L1, IGFBP4, SPARC and B2M. |
| 28498809 | 0.97 | FSTL1 contains two domains: one is a follistatin-like domain which suggests that FSTL1 is classed as the secreted protein-acidic and rich in cysteine (SPARC) family of proteins; the other one is an non-functional extracellular calcium-binding domain. |
| 31649549 | 0.97 | SPARC, FABP-3, FSTL-1, and oncostatin were analyzed using various multiplex assays. |
| 31992826 | 0.97 | FSTL1, TIMP2, FAP, SPARC, AEBP1, NOX4, and FBLN2 are known to regulate macrophage mobilization into tumor tissues, and are associated with TAM. |
| 31952198 | 0.94 | FSTL1 belongs to the secreted protein acidic and rich in cysteine (SPARC) family, which contains both extracellular calcium-binding and follistatin-like domains, and regulates cell survival, proliferation, differentiation, inflammation, and other essential processes. |
| 22247067 | 0.93 | follistatin-related protein 1 and SPARC) and insulin-like growth factor IGF-binding proteins. |
| 22675198 | 0.93 | FSTL1 is a secreted protein sharing a characteristic structural module, the follistatin domain, with follistatin, FSTL3, and members of the SPARC (secreted protein acidic and rich in cysteine) matrix protein family. |
| 28433772 | 0.92 | SPARC, FSTL1, FN1, PTX3, and LGALS1 in KM12SM cells cocultured with MSC-CM versus expression in KM12SM cells cultured alone, as determined by qRT-PCR. |
| 0.91 | secreted protein, acidic and rich in cysteine precursor (SPARC); pentraxin-related protein PTX3 precursor (PTX3); fibronectin precursor (FN1); follistatin-related protein 1 precursor (FSTL1); and galectin-1 (LGALS1) were higher in KM12SM cells directly cocultured with MSCs compared with levels in KM12SM cells cultured alone (Table 2 and Figure 2A). | |
| 29760587 | 0.92 | FSTL1, SPARC and omentin-1 in mediating insulin sensitivity in skeletal muscle have yet to be studied. |
| 30672160 | 0.92 | FSTL1 = follistatin-related protein 1, IGF1 = insulin-like growth factor 1, SPARC = secreted protein acidic and rich in cysteine, IL-6 = interleukin-6, IL-7 = interleukin-7, IL-10 = interleukin-10, IL-15 = interleukin-15 |
| 29115636 | 0.88 | Follistatin like-1 (FSTL1), also named TSC-36, located on chromosome 3, is a BM-40/SPARC/osteonectin family protein which encodes a secreted glycoprotein. |
| 31182131 | 0.88 | secreted protein, acidic, cysteine-rich (SPARC) family, which consists of SPARC, Hevin, testican-2, testican-3, and follistatin-like protein 1. |
| 25853091 | 0.87 | FSTL-1 is a TGF-beta-inducible gene, secreted protein and acidic and rich in cysteine (SPARC)-related, that enhances inflammatory cytokine/chemokine expression and also seems to be implicated in angiogenesis and revascularization. |
| 31137733 | 0.84 | SPARC, IL18, SRPX2, CCL2, PLAT, PLAU, CXCL12, SFRP2, ANGPT1, CXCL14, TGM2, FSTL1, IGFBP5, IGFBP7, LOX, and LOXL1 were diagnosed with the development of GBM. |
| 30501089 | 0.74 | SPARC, as well as less characterized ECM proteins such as MXRA5, LEPRE1, MFAP4, and FSTL1. |
| 30569103 | 0.50 | Fstl1, Fbn1 and Sparc. |
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