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pmid:34533860

LncRNA BASP1-AS1 interacts with YBX1 to regulate Notch transcription and drives the malignancy of melanoma.

YaLing Li · YaLi Gao · XueLi Niu · MingSui Tang · JingYi Li · Bing Song · XiuHao Guan

Cancer science · 2021 doi:10.1111/cas.15140

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complete

Experiment

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Data

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Analysis

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Execution

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paper object · 10 fields
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title
LncRNA BASP1-AS1 interacts with YBX1 to regulate Notch transcription and drives the malignancy of melanoma.
doi
10.1111/cas.15140
pmid
34533860
authors array · 7 items
[0]
YaLing Li
[1]
YaLi Gao
[2]
XueLi Niu
[3]
MingSui Tang
[4]
JingYi Li
[5]
Bing Song
[6]
XiuHao Guan
journal
Cancer science
year
2021
abstract
Melanoma is a fatal skin malignant tumor with a poor prognosis. We found that long noncoding RNA BASP1-AS1 is essential for the development and prognosis of melanoma. The methylation, RNA sequencing, copy number variation, mutation data, and sample follow-up information of melanoma from The Cancer Genome Atlas (TCGA) were analyzed using weighted gene co-expression network analysis and 366 samples common to the three omics were selected for multigroup clustering analysis. A four-gene prognostic model (BASP1-AS1, LOC100506098, ARHGAP27P1, and LINC01532) was constructed in the TCGA cohort and validated using the GSE65904 series. The expression of BASP1-AS1 was upregulated in melanoma tissues and various melanoma cell lines. Functionally, the ectopic expression of BASP1-AS1 promoted cell proliferation, migration, and invasion in both A375 and SK-MEL-2 cells. Mechanically, BASP1-AS1 interacted with YBX1 and recruited it to the promoter of NOTCH3, initiating its transcription process. The activation of the Notch signaling then resulted in the transcription of multiple oncogenes, including c-MYC, PCNA, and CDK4, which contributed to melanoma progression. Thus, BASP1-AS1 could act as a potential biomarker for cutaneous malignant melanoma.
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Comparison between two groups was assessed using an unpaired two‐tailed t‐test, with P < .05 being considered as statistically significant.
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Multiomics screening of LncRNA differences in melanoma subtypes
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Multiomics screening of LncRNA differences in melanoma subtypes
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Screening LncRNAs associated with prognosis of melanoma
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Significant difference in prognosis of LncRNAs
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0.753489531
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0.987114358
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6.16E‐06
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0.00888111
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Screening LncRNAs associated with prognosis of melanoma
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Four prognostic independent CNV‐related lncRNA molecules
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red at −80°C after surgery. Cell culture and transfection All cell lines were obtained from the Chines
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{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:34533860", "kind": "science-record", "revision": 7, "content_hash": "sha256:ebf47d0225c9abce2f0a8d11d5c050b5e182f6a25eed043b8761a4c7ce679817", "created_at": "2026-11-01T15:41:52Z", "updated_at": "2026-11-01T21:26:15Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "LncRNA BASP1-AS1 interacts with YBX1 to regulate Notch transcription and drives the malignancy of melanoma.", "doi": "10.1111/cas.15140", "pmid": "34533860", "authors": ["YaLing Li", "YaLi Gao", "XueLi Niu", "MingSui Tang", "JingYi Li", "Bing Song", "XiuHao Guan"], "journal": "Cancer science", "year": 2021, "abstract": "Melanoma is a fatal skin malignant tumor with a poor prognosis. We found that long noncoding RNA BASP1-AS1 is essential for the development and prognosis of melanoma. The methylation, RNA sequencing, copy number variation, mutation data, and sample follow-up information of melanoma from The Cancer Genome Atlas (TCGA) were analyzed using weighted gene co-expression network analysis and 366 samples common to the three omics were selected for multigroup clustering analysis. A four-gene prognostic model (BASP1-AS1, LOC100506098, ARHGAP27P1, and LINC01532) was constructed in the TCGA cohort and validated using the GSE65904 series. The expression of BASP1-AS1 was upregulated in melanoma tissues and various melanoma cell lines. Functionally, the ectopic expression of BASP1-AS1 promoted cell proliferation, migration, and invasion in both A375 and SK-MEL-2 cells. Mechanically, BASP1-AS1 interacted with YBX1 and recruited it to the promoter of NOTCH3, initiating its transcription process. The activation of the Notch signaling then resulted in the transcription of multiple oncogenes, including c-MYC, PCNA, and CDK4, which contributed to melanoma progression. 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