2022
DOI: 10.1016/j.biopha.2022.113019
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LINC00963: A potential cancer diagnostic and therapeutic target

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Cited by 20 publications
(10 citation statements)
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“…LINC00963 can also control four downstream protein-coding genes directly. By participating in EGFR transactivation, LINC00963 particularly promotes the transition of prostate cancer through an androgen-dependent to an androgen-independent phase (Xie et al, 2022). Based on the study of Wu et al in 2020, LINC00963 was discovered to be up-regulated in BC patients, and its presence was correlated to metastasis to "lymph node, TNM stage, and differentiation grade".…”
Section: Discussionmentioning
confidence: 99%
“…LINC00963 can also control four downstream protein-coding genes directly. By participating in EGFR transactivation, LINC00963 particularly promotes the transition of prostate cancer through an androgen-dependent to an androgen-independent phase (Xie et al, 2022). Based on the study of Wu et al in 2020, LINC00963 was discovered to be up-regulated in BC patients, and its presence was correlated to metastasis to "lymph node, TNM stage, and differentiation grade".…”
Section: Discussionmentioning
confidence: 99%
“…Safranal, a small molecule from saffron, has shown anticancer activity against HepG2 cells via oxidative stress-triggered protein destabilization and DNA damage apoptosis [ 25 ]. Moreover, mounting evidence has revealed that noncoding RNAs, such as LINC00963, show potent oncogenic effects via modulating the PI3K/AKT, Wnt, AMPK, and MAPK signaling pathways, thereby governing cell proliferation, migration, invasion, EMT, and apoptosis [ 26 ]. Adenine-induced AMPK activation has been implicated in the regulation of cell cycle progression and invasiveness of cancer cells [ 19 , 27 ]; however, the roles of oxidative stress and noncoding RNAs in adenine-mediated anticancer action need further investigation.…”
Section: Discussionmentioning
confidence: 99%
“…In addition to the above-mentioned signalling mechanisms and physiological consequences triggered by the ET-1 axis, the ET-1 GPCR receptor can activate Epidermal Growth Factor Receptor (EGFR) through an unconventional signalling process known as signal crosstalk [9,82,83]. The tumorigenicity of the EGFR activation and signalling pathway has been long studied in depth in ovary cancer head and neck cancer, colorectal cancer and breast cancer [38,[83][84][85]. EGFR and its signalling are key regulators of cellular activities such as proliferation, differentiation, apoptosis, and migration [86,87].…”
Section: Role Of Et-1 Axis In Cancermentioning
confidence: 99%