Identification of optimal reference genes for gene expression normalization in a wide cohort of endometrioid endometrial carcinoma tissues

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Abstract

Accurate normalization is a primary component of a reliable gene expression analysis based on qRT-PCR technique. While the use of one or more reference genes as internal controls is commonly accepted as the most appropriate normalization strategy, many qPCR-based published studies still contain data poorly normalized and reference genes arbitrarily chosen irrespective of the particular tissue and the specific experimental design. To date, no validated reference genes have been identified for endometrial cancer tissues. In this study, 10 normalization genes (GAPDH, B2M, ACTB, POLR2A, UBC, PPIA, HPRT1, GUSB, TBP, H3F3A) belonging to different functional and abundance classes in various tissues and used in different studies, were analyzed to determine their applicability. In total, 100 endometrioid endometrial cancer samples, which were carefully balanced according to their tumor grade, and 29 normal endometrial tissues were examined using SYBR Green Real-Time RT-PCR. The expression stability of candidate reference genes was determined and compared by means of geNorm and NormFinder softwares. Both algorithms were in agreement in identifying GAPDH, H3F3A, PPIA, and HPRT1 as the most stably expressed genes, only differing in their ranking order. Analysis performed on the expression levels of all candidate genes confirm HPRT1 and PPIA as the most stably expressed in the study groups regardless of sample type, to be used alone or better in combination. As the stable expression of HPRT1 and PPIA between normal andtumor endometrial samples fulfill the basic requirement of a reference gene to be used for normalization purposes, HPRT1 expression showed significant differences between samples from low-grade and high-grade tumors. In conclusion, our results recommend the use of PPIA as a single reference gene to be considered for improved reliability of normalization in gene expression studies involving endometrial tumor samples at different tumor degrees.

Figures

  • Table 1. Clinical and pathologic characteristics of 100 EC and 29 NE patients.
  • Table 2. Candidate reference genes selected for evaluation of expression stability.
  • Figure 1. Expression levels of candidate reference genes in malignant (hatched boxes) and nonmalignat (open boxes) endometrial samples. Values are given as calibrated normalized relative quantities (CNRQ). Boxes indicate IQR for the data of unmatched samples in each group.
  • Table 3. Fold changes in reference gene expression between malignant and non-malignant endometrial samples and among malignant samples grouped according to tumor grade and stage (90% confidence intevals, Lower and Upper bounderies; $ p-value for one-way ANOVA; R5* null hypothesis of non equivalence rejected; [eL,eU]5[0.8,1.25]).
  • Figure 2. Selection of the most suitable reference genes for normalization in endometrial cancer samples using geNorm analysis. Results are presented according to the output file of the geNorm program [11]. (A) Average expression stability value (M) of control genes calculated by a stepwise exclusion of the least stable genes: the program enables elimination of the worst-scoring gene with the highest M value and recalculation of new M value for the remaining genes. X axis from the left to the right indicates gene rank according to expression stability, while Y axis indicate the stability measure M. (B) Determination of the optimal number of control genes for normalization.
  • Table 4. Candidate reference genes for normalization listed according to their expression stability calculated by the NormFinder program.

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Romani, C., Calza, S., Todeschini, P., Tassi, R. A., Zanotti, L., Bandiera, E., … Bignotti, E. (2014). Identification of optimal reference genes for gene expression normalization in a wide cohort of endometrioid endometrial carcinoma tissues. PLoS ONE, 9(12). https://doi.org/10.1371/journal.pone.0113781

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