» Articles » PMID: 34752497

Uncovering the Stability Status of the Reputed Reference Genes in Breast and Hepatic Cancer Cell Lines

Overview
Journal PLoS One
Date 2021 Nov 9
PMID 34752497
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Accurate and reliable relative gene expression analysis via the Reverse Transcription-quantitative Real Time PCR (RT-qPCR) method strongly depends on employing several stable reference genes as normalizers. Utilization of the reference genes without analyzing their expression stability under each experimental condition causes RT-qPCR analysis error as well as false output. Similar to cancerous tissues, cancer cell lines also exhibit various gene expression profiles. It is crucial to recognize stable reference genes for well-known cancer cell lines to minimize RT-qPCR analysis error. In this study, we showed the expression level and investigated the expression stability of eight common reference genes that are ACTB, YWHAZ, HPRT1, RNA18S, TBP, GAPDH, UBC, and B2M, in two sets of cancerous cell lines. One set contains MCF7, SKBR3, and MDA-MB231 as breast cancer cell lines. Another set includes three hepatic cancer cell lines, including Huh7, HepG2, and PLC-PRF5. Three excel-based softwares comprising geNorm, BestKeeper, and NormFinder, and an online tool, namely RefFinder were used for stability analysis. Although all four algorithms did not show the same stability ranking of nominee genes, the overall results showed B2M and ACTB as the least stable reference genes for the studied breast cancer cell lines. While TBP had the lowest expression stability in the three hepatic cancer cell lines. Moreover, YWHAZ, UBC, and GAPDH showed the highest stability in breast cancer cell lines. Besides that, a panel of five nominees, including ACTB, HPRT1, UBC, YWHAZ, and B2M showed higher stability than others in hepatic cancer cell lines. We believe that our results would help researchers to find and to select the best combination of the reference genes for their own experiments involving the studied breast and hepatic cancer cell lines. To further analyze the reference genes stability for each experimental condition, we suggest researchers to consider the provided stability ranking emphasizing the unstable reference genes.

Citing Articles

Screening and validating the optimal panel of housekeeping genes for 4T1 breast carcinoma and metastasis studies in mice.

Souza J, Antunes-Porto A, da Silva Oliveira I, Amorim C, Pires L, de Brito Duval I Sci Rep. 2024; 14(1):26476.

PMID: 39488625 PMC: 11531515. DOI: 10.1038/s41598-024-77126-x.


Reference gene evaluation for normalization of gene expression studies with lymph tissue and node‑derived stromal cells of patients with oral squamous cell carcinoma.

James B, Zaidi S, Bs N, R V, Dokhe Y, Shetty V Oncol Lett. 2024; 28(5):540.

PMID: 39310029 PMC: 11413728. DOI: 10.3892/ol.2024.14673.


GC-MS analysis, molecular docking, and apoptotic-based cytotoxic effect of Caladium lindenii Madison extracts toward the HeLa cervical cancer cell line.

Kalsoom A, Altaf A, Sarwar M, Maqbool T, Ashraf M, Sattar H Sci Rep. 2024; 14(1):18438.

PMID: 39117897 PMC: 11310479. DOI: 10.1038/s41598-024-69582-2.


Selection of reference genes in liproxstatin-1-treated K562 Leukemia cells via RT-qPCR and RNA sequencing.

Dong H, Hu X, Liang S, Wang R, Cheng P Mol Biol Rep. 2024; 51(1):55.

PMID: 38165476 DOI: 10.1007/s11033-023-08912-5.


Validation of reference gene stability for miRNA quantification by reverse transcription quantitative PCR in the peripheral blood of patients with COVID-19 critical illness.

Formosa A, Acton E, Lee A, Turgeon P, Izhar S, Plant P PLoS One. 2023; 18(8):e0286871.

PMID: 37643172 PMC: 10464995. DOI: 10.1371/journal.pone.0286871.


References
1.
Ferreira E, Cronje M . Selection of suitable reference genes for quantitative real-time PCR in apoptosis-induced MCF-7 breast cancer cells. Mol Biotechnol. 2011; 50(2):121-8. DOI: 10.1007/s12033-011-9425-3. View

2.
Gorji-Bahri G, Moradtabrizi N, Vakhshiteh F, Hashemi A . Validation of common reference genes stability in exosomal mRNA-isolated from liver and breast cancer cell lines. Cell Biol Int. 2021; 45(5):1098-1110. DOI: 10.1002/cbin.11556. View

3.
Zhang G, Tang X, Liang L, Zhang W, Li D, Li X . DNA and RNA sequencing identified a novel oncogene VPS35 in liver hepatocellular carcinoma. Oncogene. 2020; 39(16):3229-3244. DOI: 10.1038/s41388-020-1215-6. View

4.
Nwosu Z, Battello N, Rothley M, Pioronska W, Sitek B, Ebert M . Liver cancer cell lines distinctly mimic the metabolic gene expression pattern of the corresponding human tumours. J Exp Clin Cancer Res. 2018; 37(1):211. PMC: 6122702. DOI: 10.1186/s13046-018-0872-6. View

5.
Chen M, Wei L, Law C, Tsang F, Shen J, Cheng C . RNA N6-methyladenosine methyltransferase-like 3 promotes liver cancer progression through YTHDF2-dependent posttranscriptional silencing of SOCS2. Hepatology. 2017; 67(6):2254-2270. DOI: 10.1002/hep.29683. View