Target intelligence / Profile preview

TAPT1 antisense RNA 1 (TAPT1-AS1)

Target
TAPT1-AS1
Molecular classification
Long non-coding RNA (lncRNA), Antisense RNA
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Overview

TAPT1 antisense RNA 1 (TAPT1-AS1) is a long non-coding RNA (lncRNA) transcribed from the antisense strand of the TAPT1 gene[1]. It does not encode a protein, but is implicated in the regulation of gene expression, including autophagy and cell survival, and has been identified with oncogenic functions in several cancer types, such as colorectal cancer and neuroendocrine prostate cancer[2][4]. TAPT1-AS1 is often upregulated in metastatic and aggressive tumors, promoting cancer cell invasion, metastasis, and angiogenesis by stabilizing the mRNA for vascular endothelial growth factor A (VEGFA)[4]. Despite its proximity and antisense orientation to TAPT1, TAPT1-AS1 does not regulate TAPT1 protein expression directly and is not involved in TAPT1-related congenital disorders[1]. TAPT1-AS1 has been proposed as a potential therapeutic target for the treatment of neuroendocrine tumors and metastatic cancers[2][4]. No approved drugs yet specifically target TAPT1-AS1, but its modulation may influence cancer cell viability and disease progression. Conflicting reports exist regarding its tumor-suppressive versus oncogenic roles in different cancer types[4].

Other names
TAPT1-AS1FLJ39653TAPT1 antisense RNA 1 (head to head)
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Mechanism of action

Drugs targeting TAPT1-AS1 would likely act via inhibition of lncRNA function, suppression of cancer cell survival, inhibition of autophagy, or disruption of angiogenic pathways

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Biological functions

Regulation of gene expressionRegulation of autophagyPromotion of angiogenesisPromotion of cell migration, invasion, and metastasisMaintenance of neuroendocrine cell survivalPossible involvement in synaptogenesisPost-transcriptional regulation of mRNA stability
04

Disease associations

Cancer (oncogenic role in colorectal cancer, ovarian cancer, cervical cancer, neuroendocrine prostate cancer)Metastasis promotion (colorectal cancer liver metastasis)Potential tumor suppressor in glioma (conflicting evidence)Not reported for inflammation, neurodegenerative disease, cardiovascular disease, or infections
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Safety considerations

Specific safety concerns or therapeutic challenges have not been reported or established for targeting TAPT1-AS1 directly
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Interacting drugs

Treatment with enzalutamide affects TAPT1-AS1 expression in prostate cancer cells
07

Biomarkers

TAPT1-AS1 expression levels (as biomarker for neuroendocrine differentiation and survival in prostate cancer, or metastasis in colorectal cancer)

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