Abstract 7346: RNA-seq analysis confirms post-thaw transcriptomic stability in ThawReady (TM) THP-1 assay-ready cells

Abstract Cryopreserved cell lines have become essential for high-throughput screening and assay development, offering convenience and consistency across experiments. However, the freeze-thaw process can induce cellular stress, potentially affecting gene expression and compromising functional reliability. To ensure consistent assay performance, it is crucial to verify that cryopreserved cells retain their transcriptomic and functional integrity after thawing. In this study, we evaluated the transcriptomic stability of ThawReady™ THP-1 (TIB-202-AR™) cells using RNA sequencing (RNA-seq). Cells were analyzed immediately after thawing (0-hour) and following 2-hour and 8-hour recovery intervals and were compared to freshly cultured THP-1 cells. Principal component and hierarchical clustering analyses revealed that post-thaw samples closely grouped with fresh controls, demonstrating preservation of cellular identity and global gene expression patterns. Gene expression profiles showed strong concordance across key immune and inflammatory pathways characteristic of THP-1 cells. Differential expression analysis identified 178 genes altered at 0 hours, 951 at 2 hours, and 713 at 8 hours post-thaw relative to fresh culture, using a threshold of absolute fold change >5 and FDR-adjusted p-value <0.05. Despite these transient changes, pathways related to cell survival and proliferation remained stable. Notably, phagosome formation was the top-enriched pathway, suggesting adaptive recovery responses that support cell viability. Overall, these results confirm that ThawReady™ THP-1 cells maintain robust transcriptomic integrity post-thaw, supporting their reliability and reproducibility for downstream immune and inflammation-related functional assays. Citation Format: Ajeet P. Singh, Utsav Sharma, Lucas Underwood, Noah Wax, Steve King, Nilay Chakraborty, Jonathan Jacobs, . RNA-seq analysis confirms post-thaw transcriptomic stability in ThawReady (TM) THP-1 assay-ready cells [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7346.

Authors

Institutions

Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7346
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Abstract 7346: RNA-seq analysis confirms post-thaw transcriptomic stability in ThawReady (TM) THP-1 assay-ready cells

Noah Wax, Jonathan L. Jacobs, Steve King, Nilay Chakraborty et al.
Cancer Research
Single-cell and spatial transcriptomics
article

Abstract 7346: RNA-seq analysis confirms post-thaw transcriptomic stability in ThawReady (TM) THP-1 assay-ready cells

Noah Wax, Jonathan L. Jacobs, Steve King, Nilay Chakraborty, Ajeet P. Singh, Utsav Sharma, Lucas Underwood
article en

Abstract

Abstract Cryopreserved cell lines have become essential for high-throughput screening and assay development, offering convenience and consistency across experiments. However, the freeze-thaw process can induce cellular stress, potentially affecting gene expression and compromising functional reliability. To ensure consistent assay performance, it is crucial to verify that cryopreserved cells retain their transcriptomic and functional integrity after thawing. In this study, we evaluated the transcriptomic stability of ThawReady™ THP-1 (TIB-202-AR™) cells using RNA sequencing (RNA-seq). Cells were analyzed immediately after thawing (0-hour) and following 2-hour and 8-hour recovery intervals and were compared to freshly cultured THP-1 cells. Principal component and hierarchical clustering analyses revealed that post-thaw samples closely grouped with fresh controls, demonstrating preservation of cellular identity and global gene expression patterns. Gene expression profiles showed strong concordance across key immune and inflammatory pathways characteristic of THP-1 cells. Differential expression analysis identified 178 genes altered at 0 hours, 951 at 2 hours, and 713 at 8 hours post-thaw relative to fresh culture, using a threshold of absolute fold change >5 and FDR-adjusted p-value <0.05. Despite these transient changes, pathways related to cell survival and proliferation remained stable. Notably, phagosome formation was the top-enriched pathway, suggesting adaptive recovery responses that support cell viability. Overall, these results confirm that ThawReady™ THP-1 cells maintain robust transcriptomic integrity post-thaw, supporting their reliability and reproducibility for downstream immune and inflammation-related functional assays. Citation Format: Ajeet P. Singh, Utsav Sharma, Lucas Underwood, Noah Wax, Steve King, Nilay Chakraborty, Jonathan Jacobs, . RNA-seq analysis confirms post-thaw transcriptomic stability in ThawReady (TM) THP-1 assay-ready cells [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 7346.

Cancer ResearchVol. 86(7_Supplement)
American Type Culture Collection (US)
Openalex Percentile: Top 31%
Single-cell and spatial transcriptomics
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.