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Min Xiao

Researcher at Huazhong University of Science and Technology

Publications -  117
Citations -  5273

Min Xiao is an academic researcher from Huazhong University of Science and Technology. The author has contributed to research in topics: Melanoma & Medicine. The author has an hindex of 27, co-authored 107 publications receiving 3966 citations. Previous affiliations of Min Xiao include University of Texas MD Anderson Cancer Center & University Hospital of Basel.

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Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance

TL;DR: It is shown that human melanoma cells can display profound transcriptional variability at the single-cell level that predicts which cells will ultimately resist drug treatment, and this work reveals the multistage nature of the acquisition of drug resistance and provides a framework for understanding resistance dynamics in single cells.
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Activation of Notch1 signaling is required for β-catenin–mediated human primary melanoma progression

TL;DR: The data suggest a beta-catenin-dependent, stage-specific role for Notch1 signaling in promoting the progression of primary melanoma, andhibiting beta-Catenin expression reversed notch1-enhanced tumor growth and metastasis.
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Increased cyclin D1 expression can mediate BRAF inhibitor resistance in BRAF V600E-mutated melanomas.

TL;DR: Increased levels of cyclin D1, resulting from genomic amplification, may contribute to the BRAF inhibitor resistance of BRAF V600E–mutated melanomas, particularly when found in the context of a CDK4 mutation/overexpression.
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Notch1 signaling promotes primary melanoma progression by activating mitogen-activated protein kinase/phosphatidylinositol 3-kinase-Akt pathways and up-regulating N-cadherin expression.

TL;DR: It is shown that Notch1 signaling drives the vertical growth phase (VGP) of primary melanoma toward a more aggressive phenotype and regulation of MAPK/PI3K-Akt pathway activities and expression of N-cadherin by the Notch pathway provides a mechanistic basis for Notch signaling in the promotion ofPrimary melanoma progression.