A dataset of chronic nicotine-induced genes in breast cancer cells

These data show the differentially expressed genes (DEG) from HCC38 breast cancer cell line chronically exposed to nicotine versus vehicle control. Additional data is also provided from dynamic trajectory analysis, identifying the most dynamic genes due to chronic nicotine treatment. To produce this dataset, we first performed single cell RNA sequencing from HCC38 cells chronically treated with vehicle or nicotine, followed by scanpy analysis to yield 6 discrete cell clusters at conservative resolution. We then evaluated differential gene expression between chronic nicotine and control cells for each individual cluster or in the whole sample using PyDESeq2. For dynamic trajectory analysis, Velocyto (0.6) was used to estimate the spliced and unspliced counts for each gene between chronic nicotine-treated cells and vehicle, allowing computation of gene velocities. These data are useful for analysing the expression of individual genes or gene velocities either in the whole sample or in the different clusters identified. Since the HCC38 cell line used in these experiments is heterogeneous, including cells with features of stem-like, luminal progenitor-like and more differentiated cells, this dataset allows examination of the conserved as well as disparate gene expression effects of nicotine in different breast cancer cell types. Our dataset has a great potential for re-use given the recent surge in interest surrounding the role tobacco-use plays in breast cancer progression.

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Publication Details

Journal
Data in Brief
Published
2025-04-22
DOI
https://doi.org/10.1016/j.dib.2025.111573
Citations
2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
1.61

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article

A dataset of chronic nicotine-induced genes in breast cancer cells

Jay S. Desgrosellier, Samson Mugisha, Richard Klemke, Shreyas Labhsetwar et al.
2 citations
Data in Brief
Single-cell and spatial transcriptomics
1.61
article

A dataset of chronic nicotine-induced genes in breast cancer cells

Jay S. Desgrosellier, Samson Mugisha, Richard Klemke, Shreyas Labhsetwar, Devam Dave
article en
2 citations

Abstract

These data show the differentially expressed genes (DEG) from HCC38 breast cancer cell line chronically exposed to nicotine versus vehicle control. Additional data is also provided from dynamic trajectory analysis, identifying the most dynamic genes due to chronic nicotine treatment. To produce this dataset, we first performed single cell RNA sequencing from HCC38 cells chronically treated with vehicle or nicotine, followed by scanpy analysis to yield 6 discrete cell clusters at conservative resolution. We then evaluated differential gene expression between chronic nicotine and control cells for each individual cluster or in the whole sample using PyDESeq2. For dynamic trajectory analysis, Velocyto (0.6) was used to estimate the spliced and unspliced counts for each gene between chronic nicotine-treated cells and vehicle, allowing computation of gene velocities. These data are useful for analysing the expression of individual genes or gene velocities either in the whole sample or in the different clusters identified. Since the HCC38 cell line used in these experiments is heterogeneous, including cells with features of stem-like, luminal progenitor-like and more differentiated cells, this dataset allows examination of the conserved as well as disparate gene expression effects of nicotine in different breast cancer cell types. Our dataset has a great potential for re-use given the recent surge in interest surrounding the role tobacco-use plays in breast cancer progression.

Data in BriefVol. 60
University of California San Diego (US)
California Breast Cancer Research Program, Tobacco-Related Disease Research Program
Good health and well-being
Openalex Percentile: Top 18%
Single-cell and spatial transcriptomics
1.61
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A dataset of chronic nicotine-induced genes in breast cancer cells — Jay S. Desgrosellier, Samson Mugisha, et al. · Data in Brief (2025) | TGRS Research Map | TGRS