2021
DOI: 10.2147/cmar.s284258
|View full text |Cite
|
Sign up to set email alerts
|

LncRNA SBF2-AS1 Promotes Diffuse Large B-Cell Lymphoma Growth by Regulating FGFR2 via Sponging miR-494-3p

Abstract: Purpose: Currently, there is no efficient and feasible method for diffuse large B-cell lymphoma (DLBCL) in clinical practice, and the main reason is the unclear pathogenesis of DLBCL, which leads to a high fatality rate of DLBCL. Methods: Therefore, it is meaningful to explore the molecular mechanism of DLBCL and find a targeted therapeutic approach from the molecular level. Results: Long non-coding RNA (lncRNA) SBF2-AS1 was highly expressed in DLBCL tissues and cell lines. Silencing of SBF2-AS1 inhibited the … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
7
0

Year Published

2021
2021
2024
2024

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 12 publications
(7 citation statements)
references
References 28 publications
0
7
0
Order By: Relevance
“…In contrast, miR-494 is known to be sponged by several lncRNAs. Suppression of miR-494 by the lncRNA PCAT29 promotes PTEN expression [27], while a similar action by the lncRNA SBF2-AS1 promotes FGFR2 expression [28]. The downregulation of NQO1 by miR-494 has been shown to inhibit the Nrf2 signaling pathway [20], and we previously reported that miR-494 induces a quiescent state in cancer cells by suppressing oxidative phosphorylation [29].…”
Section: Discussionmentioning
confidence: 98%
“…In contrast, miR-494 is known to be sponged by several lncRNAs. Suppression of miR-494 by the lncRNA PCAT29 promotes PTEN expression [27], while a similar action by the lncRNA SBF2-AS1 promotes FGFR2 expression [28]. The downregulation of NQO1 by miR-494 has been shown to inhibit the Nrf2 signaling pathway [20], and we previously reported that miR-494 induces a quiescent state in cancer cells by suppressing oxidative phosphorylation [29].…”
Section: Discussionmentioning
confidence: 98%
“…Like any other type of cancers, the un-controlled growth and metathetic ability of DLBC lead to the high recurrent and mortality rate of the disease [18][19][20]. Therefore, an effective molecular therapeutic target of DLBC should be a key regulator that affect the proliferation and migration of the DLBC cells.…”
Section: Discussionmentioning
confidence: 99%
“…Of interest, by transferring those lncRNAs from chemoresistance GBM tissue or culture to a chemosensitive one, the chemo-sensitive tissue becomes chemoresistant [33] The lncRNA SBF2-AS1 gene is located on chromosome 11p15.1. The proliferation or invasion of many tumor types are associated with altered lncRNA SBF2-AS1 serum levels; Diffuse large B-cell lymphoma, colorectal cancer, hepatocellular carcinoma, serous ovarian carcinoma, clear cell renal cell carcinoma, esophageal squamous cell carcinoma, and lung cancer are associated with increased SBF2-AS1 serum levels [109][110][111][112][113][114][115], while laryngeal squamous cell carcinoma [116] is associated with decreased levels. LncRNA SBF2-AS1 can indirectly alter gene expression by acting as a ceRNA.…”
Section: Long Noncoding Rnas As Serum Biomarkers For Gbm Responsivene...mentioning
confidence: 99%
“…LncRNA SBF2-AS1 can indirectly alter gene expression by acting as a ceRNA. LncRNA SBF2-AS1 binds to protective miRNAs, thus inducing tumor proliferation and invasion [109][110][111]. In contrast, lncRNA SBF2-AS1 acts as an anti-oncogene in laryngeal squamous cell carcinoma by targeting a different miRNA associated with laryngeal cancer invasion and migration [116].…”
Section: Long Noncoding Rnas As Serum Biomarkers For Gbm Responsivene...mentioning
confidence: 99%