Time-course liver microarray data from 0 to 14 days in a 70% partial hepatectomy mouse model

The liver is capable of regeneration, regaining mass through compensatory hypertrophy even after resecting 70% of its mass. However, the underlying regenerative mechanism remains poorly understood. Thus, in this study, microarray data were procured over time, from 0 to 14 days post-70% partial hepatectomy (PH) in mice. This dataset was correlated with the body weight and liver weight measured at the time of liver harvest, allowing us to determine the progress of compensatory hypertrophy in each sample. Furthermore, the impact of individual differences in regenerative capacity was analyzed by preparing three biological replicates at each time point. The microarray data were confirmed to be of high quality based on the RNA integrity number and QC stats of the dataset. The reliability of the dataset was further supported by the results of hierarchical clustering and the expression variation of cell cycle-related genes. This microarray data will contribute to the elucidation of the regenerative mechanism in the 70% PH model.

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Publication Details

Journal
Scientific Data
Published
2025-05-10
DOI
https://doi.org/10.1038/s41597-025-05128-z
Citations
1
Primary Topic
Liver physiology and pathology
Type
article
Field-Weighted Citation Impact
1.32

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article

Time-course liver microarray data from 0 to 14 days in a 70% partial hepatectomy mouse model

Rika Hagiwara, Yoshinao Oki, Koichiro Kano, Takashi Nishi
1 citations
Scientific Data
Liver physiology and pathology
1.32
article

Time-course liver microarray data from 0 to 14 days in a 70% partial hepatectomy mouse model

Rika Hagiwara, Yoshinao Oki, Koichiro Kano, Takashi Nishi
article en
1 citations

Abstract

The liver is capable of regeneration, regaining mass through compensatory hypertrophy even after resecting 70% of its mass. However, the underlying regenerative mechanism remains poorly understood. Thus, in this study, microarray data were procured over time, from 0 to 14 days post-70% partial hepatectomy (PH) in mice. This dataset was correlated with the body weight and liver weight measured at the time of liver harvest, allowing us to determine the progress of compensatory hypertrophy in each sample. Furthermore, the impact of individual differences in regenerative capacity was analyzed by preparing three biological replicates at each time point. The microarray data were confirmed to be of high quality based on the RNA integrity number and QC stats of the dataset. The reliability of the dataset was further supported by the results of hierarchical clustering and the expression variation of cell cycle-related genes. This microarray data will contribute to the elucidation of the regenerative mechanism in the 70% PH model.

Scientific DataVol. 12(1)
Nihon University (JP), Fujita Health University (JP)
Ministry of Education, Culture, Sports, Science and Technology
Openalex Percentile: Top 21%
Liver physiology and pathology
1.32
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