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Ying Yang

Researcher at Sichuan University

Publications -  16
Citations -  147

Ying Yang is an academic researcher from Sichuan University. The author has contributed to research in topics: Medicine & Lung cancer. The author has an hindex of 3, co-authored 5 publications receiving 19 citations.

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Deciphering cell lineage specification of human lung adenocarcinoma with single-cell RNA sequencing.

TL;DR: The data identified a new mechanism in LUAD evolution, provided a robust basis for diagnosis and treatment of LUAD, and identified new markers including miRNA10 and β-hydroxybutyric acid to diagnose early-stage LUAD noninvasively in the blood.
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miR-15a-5p inhibits metastasis and lipid metabolism by suppressing histone acetylation in lung cancer.

TL;DR: A novel mechanism of miR-15a-5p is unveiled in inhibiting metastasis of lung cancer cells by suppressing lipid metabolism via suppression of ACSS2 mediated acetyl-CoA activity and histone acetylation.
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FRK plays an oncogenic role in non-small cell lung cancer by enhancing the stemness phenotype via induction of metabolic reprogramming.

TL;DR: FRK plays an oncogenic role in lung cancer cells via a novel regulation mechanism of enhancing the stemness of H1299 cells by inducing metabolism reprogramming, which finally promotes EMT and metastasis and indicates that FRK could be used as a potential therapeutic target for drug development.
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The heterogeneous immune landscape between lung adenocarcinoma and squamous carcinoma revealed by single-cell RNA sequencing

TL;DR: In this article , the authors performed scRNA-seq on 72,475 immune cells from 40 samples of tumor and matched adjacent normal tissues spanning 19 NSCLC patients, and drew a systematic immune cell transcriptome atlas.
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Integrated single-cell RNA sequencing analysis reveals distinct cellular and transcriptional modules associated with survival in lung cancer

TL;DR: In this article , a multi-omics atlas integrating 52 single-cell RNA sequencing and 2342 public bulk RNA sequencing was established, which revealed that LUAD and LUSC contained amplifications occurring selectively in subclusters of AT2 and basal cells.