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CD27 antisense RNA 1 (CD27-AS1)

Target
CD27-AS1
Molecular classification
Long non-coding RNA (lncRNA), Antisense RNA, Nuclear RNA
01

Overview

CD27 antisense RNA 1 is a long non-coding RNA located on chromosome 12p13.31, transcribed antisense to the CD27 gene (a key T-cell co-stimulatory receptor). It is primarily localized in the nucleus and acts as a regulator of gene expression in cancer cells. Mechanistically, CD27-AS1 serves as a ceRNA by sponging microRNAs (such as miR-224-5p in AML), thereby upregulating oncogenic factors like PBX3, promoting cell proliferation, and inhibiting apoptosis. In melanoma, the CD27-AS1-208 isoform facilitates tumor growth and invasiveness by enhancing STAT3 phosphorylation and JAK-STAT signaling. High levels of CD27-AS1 are associated with poor prognosis and aggressive disease in AML, melanoma, and potentially other cancers, making it a candidate for therapeutic targeting and biomarker development.

Other names
CD27-AS1CD27 antisense RNA 1 (non-protein coding)CD27-AS1-208
02

Mechanism of action

Drugs indirectly interacting with CD27-AS1, such as STAT3 inhibitors, would dampen STAT3 activity, potentially suppressing the proliferative effect mediated by CD27-AS1-208 in melanoma. In AML, lncRNA-targeted therapeutic strategies (e.g., antisense oligonucleotides, RNAi, CRISPR) could be designed to inhibit CD27-AS1 and its oncogenic ceRNA effects.

03

Biological functions

Regulation of cell proliferation (promotes proliferation of cancer cells in AML and melanoma)Cell cycle regulation (affects G0/G1 arrest in AML cells)Apoptosis inhibition (suppresses programmed cell death in cancer cells)Competing endogenous RNA (ceRNA) activity (sponges microRNAs such as miR-224-5p; affects gene expression of PBX3 in AML, and interacts with STAT3 pathway in melanoma)Activation of JAK-STAT signaling (enhances STAT3 phosphorylation and signaling)
04

Disease associations

Cancer (Acute myeloid leukemia)Cancer (Melanoma)Cancer (Colon adenocarcinoma [prognostic association])Potential roles in other tumors (up-regulated across TCGA data in multiple cancer types)
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Safety considerations

Delivery specificity (for CD27-AS1-targeted therapy)Off-target effects (for CD27-AS1-targeted therapy)Potential interference with immune regulation (due to proximity to CD27 gene)
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Interacting drugs

STAT3 inhibitors (indirectly relevant for tumors with CD27-AS1 upregulation)
07

Biomarkers

High expression of CD27-AS1 is a prognostic biomarker in AML (patients with elevated CD27-AS1 have significantly shorter survival)Biomarker for melanoma progression and poor prognosisBiomarker for poor prognosis in colon adenocarcinoma

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