2020
DOI: 10.1007/s13577-020-00422-x
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The interaction between MALAT1 target, miR-143-3p, and RALGAPA2 is affected by functional SNP rs3827693 in breast cancer

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Cited by 18 publications
(10 citation statements)
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“…Although the majority of proteins are shared identifications between BC patient and healthy control groups (~82%), as well as the databases we used, interestingly, we found 11 proteins which are uniquely identified only from BC patient using NanoPoms preparation (Supplementary Table s3 ). Those proteins have previously been reported to be associated with bladder cancer metastases, including IRAK4 58 , KRT23 59 , and RALGAPA2 60 (full list in Supplementary Table s3 ). Also 4 proteins were found uniquely in the healthy group using NanoPoms preparation, but not in cancer patients.…”
Section: Resultsmentioning
confidence: 99%
“…Although the majority of proteins are shared identifications between BC patient and healthy control groups (~82%), as well as the databases we used, interestingly, we found 11 proteins which are uniquely identified only from BC patient using NanoPoms preparation (Supplementary Table s3 ). Those proteins have previously been reported to be associated with bladder cancer metastases, including IRAK4 58 , KRT23 59 , and RALGAPA2 60 (full list in Supplementary Table s3 ). Also 4 proteins were found uniquely in the healthy group using NanoPoms preparation, but not in cancer patients.…”
Section: Resultsmentioning
confidence: 99%
“…Genetic variation of lncRNA may have an important role in disease susceptibility via affecting lncRNA binding capacity to proteins or miRNA and their loop structure (Guo et al, 2016;Chen et al, 2018;Fattahi Dolatabadi et al, 2020;Feng et al, 2020;Fu et al, 2020). For example, the interaction between MALAT1 target, miR-143-3p, and RALGAPA2 is affected by a functional SNP rs3827693 in breast cancer (Fattahi Dolatabadi et al, 2020). The SNP rs12982687 affects binding capacity of lncRNA UCA1 to miR-873-5p (Fu et al, 2020).…”
Section: Discussionmentioning
confidence: 99%
“…Such overexpressed MALAT1 can promote BC proliferation and progression by repressing various RNA molecules. For example, it can competitively bind with miR-1 and thereby affect the expression of CDC42 [ 189 ], downregulate hsa-miR-448, lead to aberrant expression of KDM5B [ 190 ], and regulate the expression of miR-143-3p and its putative target, RALGAPA2 [ 191 ]. Huang et al detected the MALAT1 expression levels in tissue samples collected from 20 BC patients and 20 healthy controls and found significantly higher expression levels in the former collective ( p < 0.05).…”
Section: Lncrnas In Female-oriented Cancersmentioning
confidence: 99%