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203
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"The candidate epigenetically deregulated lncRNAs CACNA1G-AS1, F11-AS1, NNT-AS1, and MSC-AS1 might function as key regulatory factors in the development and progression of PC and could be potential therapeutic and prognostic biomarkers for PC, which were associated with the poor prognosis of the patients with PC."
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"Out of 24 pairs, a significant negative correlation [correlation coefficient (R) > − 0.3 and p-value < 0.05] was observed between the 8 DElncRNA (BMS1P4, CACNA1G-AS1, MIR9-3HG, SDK1-AS1, PPM1K-DT, F11-AS1, NNT-AS1, and MSC-AS1) and their respective 8 DMCs (cg19500311, cg23614229, cg00576773, cg23194354, cg05850997, cg23957912, cg12626968, and cg11052780) (Figs. xref and xref )."
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"A significant inverse correlation was found between the promoter methylation (cg19500311, cg23614229, cg00576773, cg23194354, cg05850997, cg23957912, cg12626968, and cg11052780) of 8 corresponding aberrantly expressed DElncRNAs (BMS1P4, CACNA1G-AS1, MIR9-3HG, SDK1-AS1, PPM1K-DT, F11-AS1, NNT-AS1, and MSC-AS1)."
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"Among lncRNAs with diagnostic and prognostic values, HOTAIR, xref , xref , xref HOTTIP, xref PEG10, xref , xref LUNAR1, xref HULC, xref TUG1, xref TRIM52‐AS1, xref TRERNA1, xref CACNA1G‐AS1 xref and SNHG16 xref were upregulated, but NONHSAT120161, xref GAS5, xref OR2A1‐ AS1 xref , xref and PANDA xref were downregulated."
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"Finally, we performed multivariate Cox regression analysis for five optimal lncRNA biomarkers and constructed a lncRNA-based risk score model based on the linear combination of the expression of five optimal lncRNA biomarkers, weighted by their coefficients from the multivariate regression analysis as follows: EpiLncRNASig = (0.197) ∗ expression ( LINC00189 ) + (0.167) ∗ expression ( CACNA1G-AS1 ) + (−0.432) ∗ expression ( AL133467.1 ) + (−0.374) ∗ expression ( CHRM3-AS2 ) + (0.395) ∗ expression ( AC105384.1 )."
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"As shown in xref , three lncRNAs ( LINC00189 , CACNA1G-AS1 , and AC105384.1 ) revealed significantly higher expression in the high-risk group compared to those in the low-risk group, and two lncRNAs ( AL133467.1 and CHRM3-AS2 ) are significantly upregulated in the low-risk group and down-regulated in the high-risk group ( xref )."
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"By analyzing CACNA1G-AS1 expression levels in 122 pairs of non-small cell lung cancer (NSCLC) and normal tissue samples as well as in NSCLC cell lines, xref identified CACNA1G-AS1 as an oncogene to promote cell migration, invasion, and epithelial-mesenchymal transition via regulating HNRNPA2B1 ."
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"A recent study performed by Wei revealed higher expression of CACNA1G-AS1 in colorectal cancer (CRC) tissues compared to adjacent normal tissues and found that CACNA1G-AS1 was able to enhance proliferative and invasive abilities of CRC cells by downregulating p53 via forming a carcinogenic complex with EZH2 ( xref )."
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"Two additional ncRNAs were also shown to affect p53 levels: the lncRNA CACNA1G-AS1, which decreases p53 levels, is more highly expressed in CRC tissues than in adjacent normal tissue, whereas the circular RNA, circZNF609, which enhances p53 levels, shows decreased expression in CRC compared with adjacent normal tissue [ xref , xref ]."
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"The study on aberrantly expressed lncRNAs in ALCL identified five lncRNAs, which were highly expressed in ALCL, including ~5, ~10, ~15, ~17, and ~19-fold for CACNA1G-AS1, BMS1P20, RNF144A-AS1, LINC01013, and MIR503HG, respectively. xref Among these, the function of LINC01013 has been validated in tumor cell invasion, however, no recent studies have reported an interaction between other lncRNAs and progression of ALCL. xref Pan et al identified 189 differentially expressed lncRNAs in FL compared to reactive lymphatic nodes tissues (>10 fold). xref ENST00000572608, ENST00000545410 (RP11-625 L16.3), and ENST00000433406 (CTC-546 K23.1) showed a significant high expression, suggesting their potential role in the pathogenesis of FL. xref Moreover, plenty of unknown lncRNAs, including AC00196.1, RP11-12A2.3, AF127936.5, AC010983.1, and RP11-530N7.3 has been identified in MCL, which needs their pathological role to be clear. xref "
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"It can be observed that LBX2-AS1 has a significant positive correlation with a variety of immune infiltrating cells, such as Activated dendritic cell, Macrophage and Central memory CD8 T cell, and CACNA1G-AS1 has a significant negative correlation with a variety of immune infiltrating cells, such as Type 17 T helper cell, Immature dendritic cell and Activated dendritic cell ( xref )."
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"Furthermore, a lncRNA-based risk score was developed by integrating the expression data for these 11 lncRNAs with corresponding coefficients weighted by the LASSO model as follows: Risk score = (0.147 × LINC02408 expression value) + (-0.066 × LINC00488 expression value) + (-0.161 × LINC00337 expression value) + (0.104 × Z98257.1 expression value) + (-0.129 × CHRM3-AS2 expression value) + (-0.14 × C4A-AS1 expression value) + (-0.156 × AC104667.2 expression value) + (0.088 × AC087521.1 expression value) + (-0.159 × SOCS2-AS1 expression value) + (0.096 × AC010275.1 expression value) + (0.111 × CACNA1G-AS1 expression value)."
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"Microarray profiling of long noncoding RNAs (lncRNAs) has also been performed in lesional keloid tissue, identifying altered expression of CACNA1G-AS1 and HNF1A-AS1, which interact not only with pro-fibrotic TGF-β pathways, but also with cellular adhesion and tight junction signaling [ xref , xref ]."
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"The results revealed that the contents of CACNA1G-AS1 and FTH1 in IGF2BP1 samples treated with AGO2 showed obvious enrichment compared with those treated with IgG, while the contents of CACNA1G-AS1 and FTH1 in AGO2 samples treated with IGF2BP1 were significantly enriched compared with those in samples treated with mimics-NC."
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"First, we detected the colocalization of ferritin and lysosome labels, and the results confirmed that the colocalization of ferritin (FTH1) and lysosome (LAMP2) significantly increased in CACNA1G-AS1 knockdown ovarian cancer cells, while IGF2BP1 upregulation reversed this change."
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"The results showed that overexpressed CACNA1G-AS1 could upregulate FTH1 and GPX4, while IGF2BP1 downregulation could reverse this change ( xref and xref ); moreover, CACNA1G-AS1 knockdown could downregulate FTH1 and GPX4 expression, while IGF2BP1 upregulation could rescue this effect ( xref and xref )."
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"CACNA1G‐AS1 promoted the progression of HCC via competitively binding miR‐2392 and alleviating its inhibition on C1orf61. xref MCM3AP‐AS1 promoted the expression of FOXA1 through targeting miR‐194‐5p and thus exerted an oncogenic role in HCC. xref DSCR8 facilitated the activation of the Wnt/β‐catenin signaling pathway in HCC via the DSCR8/miR‐485‐5p/FZD7 axis. xref A few studies identified HCC‐related potential prognostic biomarkers via the construction of the ceRNA network. xref , xref , xref However, they were based on online tools that failed to take complex interactions among genes or disease‐specific data features into account."
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"The observation of mitochondrial morphology revealed that in CACNA1G-AS1 knockdown ovarian cancer cells, the mitochondrial volume was obviously reduced, the mitochondrial membrane was ruptured and the cristae vanished, while these changes could be rescued by IGF2BP1 and FTH1 overexpression ( xref )."
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"The subcutaneous tumor transplantation experiment showed that compared with that in tumor-bearing mice treated with SKOV3 cells and FAC, the growth rate of tumors in vivo significantly slowed ( xref ), while the tumor weight and volume were obviously reduced ( p < 0.01, xref and xref ) in tumor-bearing mice injected with CACNA1G-AS1 knockdown SKOV3 cells and FAC."
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"Jianfeng Zheng etc. conduct a four m6A-related lncRNAs prognostic signature (AC010894.3, ACAP2-IT1, CACNA1G-AS1 and UBA6-AS1) for predicting the prognosis of OC patients based on the training dataset, while we built a m6A-related lncRNAs prognostic signature containg seven lncRNAs."
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"According to the least absolute shrinkage and selection operator (LASSO) Cox regression analysis of these ten lncRNAs, they then conducted a prognostic signature containing four m 6 A-mediated lncRNAs (AC010894.3, ACAP2-IT1, CACNA1G-AS1 and UBA6-AS1), which shows great predictive value in ovarian cancer detection [ xref ]."
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"Additionally, Y Song et al. established a nomogram based on the expression level of seven m 6 A-related lncRNAs (AC008669.1, AC010336.1, AC097376.3, AC130710.1, ACAP2-IT1, AL138820.1 and CACNA1G-AS1) to predict survival rate of patients with ovarian cancer, revealing that m 6 A-related lncRNAs may act an important role in ovarian cancer treatment [ xref ]."