Proteomics

Dataset Information

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LncRNA LINC00622 directly bingding proteins in melanoma cells


ABSTRACT: We conducted an RNA pulldown assay in melanoma cell line SK-MEL-28 using in vitro-transcribed full-length LINC00622 RNA accompanied with a control EGFP RNA. The specific binding proteins of LINC00622 was identified using high-performance liquid chromatography-mass spectrometry (HPLC-MS).

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Melanocyte, Skin

DISEASE(S): Skin Melanoma

SUBMITTER: can li  

LAB HEAD: can Li

PROVIDER: PXD055040 | Pride | 2025-07-21

REPOSITORIES: Pride

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Publications

LINC00622 transcriptionally promotes RRAGD to repress mTORC1-modulated autophagic cell death by associating with BTF3 in cutaneous melanoma.

Li Can C   Wang Ke K   Zhao Lei L   Liu Jieyu J   Jin Yi Y   Zhang Chunting C   Xu Minna M   Wang Min M   Kuang Yanjie Y   Liu Jun J   Zhou Liang L   Wen Qian Q  

Cell death & disease 20250712 1


Autophagy plays critical and complicated roles in tumors. As the central hub of nutrient signaling and cell growth, mTOR constitutes mTORC1 to be the main gateway for modulating autophagy. Yet, the regulatory mechanisms of mTORC1-regulated autophagy in tumors are not fully deciphered. Here, we report a novel long noncoding RNA, LINC00622, which modulates mTORC1-regulated autophagy in cutaneous melanoma. Functionally, LINC00622 acts as a pro-oncogenic factor to promote proliferation, colony forma  ...[more]

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