Comprehensive Expression Profiling and Molecular Basis of CDC28 Protein Kinase Regulatory Subunit 2 in Cervical Cancer

Qin, Li; Luo, Xiaoqiong; Qin, Xiao; Huang, Hongbao; Zhang, Lianling; Chen, Shengcai; Wu, Xiaoqin; Huang, Bingsheng; Pan, Jian; Wei, Jingxi

doi:https://doi.org/10.1155/2022/6084549

International Journal of Genomics

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Abstract Introduction Materials and Methods Results Discussion Conclusion Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2022 | Article ID 6084549 | https://doi.org/10.1155/2022/6084549

Comprehensive Expression Profiling and Molecular Basis of CDC28 Protein Kinase Regulatory Subunit 2 in Cervical Cancer

Li Qin,¹Xiaoqiong Luo,¹Xiao Qin,²Hongbao Huang,¹Lianling Zhang,¹Shengcai Chen,¹Xiaoqin Wu,³Bingsheng Huang,¹Jian Pan,⁴and Jingxi Wei¹

Academic Editor: Luca Falzone

Received05 Mar 2022

Accepted27 Jun 2022

Published28 Jul 2022

Abstract

More and more evidence suggests the oncogenic function of overexpressed CDC28 protein kinase regulatory subunit 2 (CKS2) in various human cancers. However, CKS2 has rarely been studied in cervical cancer. Herein, taking advantage of massive genetics data from multicenter RNA-seq and microarrays, we were the first group to perform tissue microarrays for CKS2 in cervical cancer. We were also the first to evaluate the clinical significance of CKS2 with large samples (980 cervical cancer cases and 422 noncancer cases). We further excavated the mechanism of the tumor-promoting activities of CKS2 in cervical cancer through analysis of genetic mutation profiles, Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) significant enrichment of genes coexpressed with CKS2. According to the results, expression data from multilevels unanimously supported the overexpression of CKS2 in cervical cancer. Patients with cervical cancer in stage II from inhouse microarrays had significantly higher expression of CKS2, and CKS2 overexpression had an adverse impact on the disease-free survival status of cervical cancer patients in GSE44001. Both mutation types of mRNA high and mRNA low appeared in cervical cancer cases from the TCGA Firehose project. Gene coexpressed with CKS2 participated in pathways including the cell cycle, estrogen signaling pathway, and DNA replication. In summary, upregulated CKS2 is closely associated with the malignant clinical development of cervical cancer and might serve as a valuable therapeutic target in cervical cancer.

1. Introduction

Cervical cancer is notorious as one of the most renowned malignant tumors in gynecology, with a high incidence in postmenopausal women [1]. There is a tendency for younger pathogenetic ages [2]. The latest statistics show that cervical cancer ranks as the fourth most common cancer in the worldwide female population, causing 604,127 newly diagnosed cases and 341,831 deaths in 2020 [3]. Multiple factors, such as premature sexual behavior, multiple personality partners, early marriage and early childbirth, multiple childbirth, smoking, and HIV infection, could raise the risk of cervical cancer [4]. Significant advances have been made in screening tests and treatment strategies, including chemotherapy and radiotherapy [5, 6]. An increasing amount of evidence suggests the benefits of the clinical application of a multidisciplinary approach to the management of female tumors, which helps improve the quality of life of patients [7–9]. However, metastasis or recurrence frequently occurs in a part of cervical cancer patients receiving the above treatment, and the prognosis of these patients is poor [10, 11]. Hence, looking for a new way of treatment has been the focus of long-term research in cervical cancer research.

CDC28 protein kinase regulatory subunit 2 (CKS2) is a member of the CKS family, which plays crucial roles in diverse biological activities and mediates the transition of cell cycles [12]. Increasing evidence suggests the oncogenic function of overexpressed CKS2 in various human cancers, including adrenocortical carcinoma, tongue squamous cell carcinoma, lung adenocarcinoma, and hepatocellular carcinoma [13–16]. Transcriptomic analysis by Yang et al. revealed the significant prognostic value of CKS2 for adrenocortical carcinoma [13]. Gao et al. reported that inhibiting CKS2 expression in tongue squamous cell carcinoma could result in retarded cell growth and G2/M arrest in tumor cells [14]. The upregulation of CKS2 in lung adenocarcinoma was related to worse survival of patients and larger tumor size [15]. Similarly, upregulated CKS2 was observed to facilitate the malignant phenotype of hepatocellular carcinoma [16]. In light of the importance of CKS2 as a hallmark for a broad type of tumor, it is worth investigating the clinicopathological significance and molecular mechanism of CKS2 in cervical cancer.

CKS2 has rarely been studied in cervical cancer. Therefore, we aimed to systematically appraise the clinicopathological significance and explore the molecular bases of CKS2 in cervical cancer. For this, we used multiple detection technologies, including microarrays, RNA-seq, and immunohistochemistry (IHC).

2. Materials and Methods

2.1. Inhouse Tissue Microarray

In all, 124 cervical tissue samples were gathered by Panspectrum Biotechnology Limited Company, including 62 cervical cancer specimens and 62 noncancer cervix specimens (including mucosal inflammation and normal cervix tissues). Based on the judging criteria of the International Federation of Gynecology and Obstetrics, 31 cervical cancer patients were in stage I, and 31 cervical cancer patients were in stage II. Thirty-one cervical cancer patients were diagnosed with a T1 tumor according to the TNM staging published by the American Joint Committee on Cancer and Union International Center of Cancer. There was no distant metastasis or lymph node metastasis in any of the cases. All patients signed informed consent forms, and the ethics committee of the First Affiliated Hospital of Guangxi Medical University (approval ID: 2020(KY-E-095)) gave authority to the study.

The filtering of research objects, detailed procedures of IHC experiments, and the assessment rules of protein expression levels in tissue slides were described in an earlier study [17]. The antibody for CKS2 (https://www.abcam.cn/cks2-antibody-epr79462-ab155078.html) was used for incubation.

2.2. Additional Evidence from Other Microarrays and RNA-seq Datasets

Clinical data of cervical cancer patients and gene expression values (in the data format of fragments per kilobase per million or transcripts per kilobase million) in cervical cancer and noncancer cervix tissues were imported from The Cancer Genome Atlas (TCGA) database and the Genotype-Tissue Expression (GTEx) project. The incorporated dataset of the TCGA-GTEx expression matrix (containing 53 cervical adenocarcinomas, 253 cervical squamous cell carcinoma (CESC), and 14 noncancer samples) was normalized by the formula of log2 (transcripts per kilobase million value +0.001). Microarray datasets in the Gene Expression Omnibus (GEO) or ArrayExpress databases with a gene expression matrix of no less than three cervical cancers and three noncancer cervix samples belonging to Homo sapiens (before 11 June 2021) were other sources for expression analysis in the current study.

2.3. Comprehensive Expression Analysis for CKS2 Utilizing Tissue Microarray, External RNA-seq, and Microarray Datasets

The extraction and processing of CKS2 expression data were conducted according to the methods in prior work [18]. Microarrays were aggregated by the GPL platform, and the batch effect was removed for microarrays from the same platform through the limma package loaded with R software v. 3.6.1. Protein expression and diagnostic data of CKS2 from the IHC scores of tissue microarrays were appended to the volume of other public microarray and RNA-seq datasets. The standard mean deviation (SMD) plot was calculated to comprehensively evaluate the different expressions of CKS2 in cervical cancer versus noncancer tissues. The corresponding summarized receiver’s operating characteristic (SROC) curves were painted. The steps of drawing SMD forest plots and SROC curves are found in previous studies [19].

2.4. Survival Analysis of CKS2 in Cervical Cancer

The effect of CKS2 expression on the prognostic situation of cervical cancer patients from the GSE44001 and RNA-seq datasets (overall survival plus disease-free survival) was estimated with Kaplan-Meier survival curves. Such curves were created with GEPIA and GraphPad Prism and a log-rank value. The hazard ratio (HR) was calculated. The median CKS2 expression value was the threshold for grouping patients, and means statistical significance.

2.5. The Landscape of the Genetic Mutation of CKS2 in Cervical Cancer

We used the cBioPortal database to examine mutation types and -scores of mRNA expression (log RNA Seq V2 RSEM) of CKS2 in 310 cervical cancer samples with mutation data from the GDAC Firehose project.

2.6. Characterization of the Molecular Function of CKS2-Coexpressed Genes in Cervical Cancer

We carried out differential expression analysis for the expression matrix of cervical cancer from all included microarrays with the limma package loaded in the R software v.3.6.1. Differentially expressed genes (DEGs) in the RNA-seq dataset were calculated with a count matrix from the voom algorithm in R software v. 3.6.1. DEGs of cervical cancer were genes that showed aberrant expression within cervical cancer and noncancer cervix specimens ( or <-1 and adjusted ) in no less than two datasets of RNA-seq or microarrays. The association between gene expression values was appraised through a Pearson correlation test embedded in the psych package loaded by R software v. 3.6.1. Upregulated DEGs that were positively correlated with the expression of CKS2 (, adjusted ) in one or more than one dataset of cervical cancer were regarded as genes positively related to CKS2 in cervical cancer. Downregulated DEGs that had a negative relationship with CKS2 (adjusted , ) in one or more than one datasets of cervical cancer were defined as genes negatively correlated with CKS2 in cervical cancer. Functional enrichment of the above genes with significant relationships to CKS2 was annotated with the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis and Gene Ontology (GO). Functional annotation was conducted with the ClusterProfiler package loaded in R software v. 3.6.1, and adjusted was the cutoff value for significant KEGG and GO terms.

2.7. Statistical Analysis

SPSS 22.0 and GraphPad Prism v. 8.0.1 were applied to analyze inhouse tissue microarray data. At last, statistical significance was indicated by . An independent sample -test was used to compare CKS2 expression in cervical cancer patients from tissue microarrays with different clinicopathological variables.

3. Results

3.1. CKS2 Expression in Cervical Cancer from Tissue Microarrays

CKS2 was significantly upregulated in 62 cervical cancer tissues in contrast to 62 noncancer tissues () (; ) (Figures 1 and 2). IHC staining pictures reflected moderate or high immunoreactivity of CKS2 in the cancer nests of cervical cancer samples. In contrast, immunostaining of CKS2 exhibited negative or low reactivity in non-cancer cervix tissues (Figure 3). Moreover, CKS2 expression in cervical cancer patients diagnosed to be in clinical stage II () was higher compared with that in cervical cancer patients with clinical stage I () () (Figure 4).

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Figure 1

CKS2 expression in cervical cancer and noncancer samples from inhouse tissue microarrays, external microarrays, and RNA-seq datasets. (a) Violin plots for GPL570. (b) Violin plots for GPL571. (c) Violin plots for GPL6244. (d) Violin plots for GPL96. (e) Violin plots for GSE138080. (f) Violin plots for GSE26342. (g) Violin plots for GSE39001 (GPL201). (h) Violin plots for GSE4482 (GPL3515). (i) Violin plots for GSE4482 (GPL4926). (j) Violin plots for GSE46857. (k) Violin plots for GSE55940. (l) Violin plots for GSE7410. (m) Violin plots for TCGA-GTEx datasets (n). Violin plots for inhouse microarray. The expression shown in blue is for individuals without cancer, and the expression shown in red is for individuals with cancer.

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Figure 2

The discriminatory ability of CKS2 expression in distinguishing cervical cancer from noncancer tissues in each microarray and RNA-seq dataset. (a) ROC curves for GPL570. (b) ROC curves for GPL571. (c) ROC curves for GPL6244. (d) ROC curves for GPL96. (e) ROC curves for GSE138080. (f) ROC curves for GSE26342. (g) ROC curves for GSE39001 (GPL201). (h) ROC curves for GSE4482 (GPL3515). (i) ROC curves for GSE4482 (GPL4926). (j) ROC curves for GSE46857. (k) ROC curves for GSE55940. (l) ROC curves for GSE7410. (m) ROC curves for TCGA-GTEx datasets. (n) ROC curves for inhouse microarray.

Figure 3

IHC staining of CKS2 in cervical cancer and noncancer tissues from tissue microarrays. (a) Moderate staining of CKS2 in cervical squamous cell carcinoma tissues (100x). (b) Moderate staining of CKS2 in cervical squamous cell carcinoma tissues (200x). (c) Moderate staining of CKS2 in cervical squamous cell carcinoma tissues (400x). (d) Strong staining of CKS2 in cervical squamous cell carcinoma tissues (100x). (e) Strong staining of CKS2 in cervical squamous cell carcinoma tissues (200x). (f) Strong staining of CKS2 in cervical squamous tissues (400x). (g) Negative staining of CKS2 in noncancer squamous epithelium tissues (100x). (h) Negative staining of CKS2 in noncancer squamous epithelium tissues (200x). (i) Negative staining of CKS2 in noncancer squamous epithelium tissues (400x). (j) Negative staining of CKS2 in noncancer squamous epithelium (100x). (k) Negative staining of CKS2 in noncancer squamous epithelium tissues (200x). (l) Negative staining of CKS2 in noncancer squamous epithelium tissues (400x).

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3.2. CKS2 Overexpression in Cervical Cancer Samples from All Sources

The process of screening qualified RNA-seq and microarrays for comprehensive expression analysis is depicted in Figure 5. There were 19 microarrays from the GEO database (14 microarrays after being merged by the GPL platform) included for comprehensive expression analysis. A summary of the basic elements of all included microarrays is listed in Table 1. Rich samples of 781 cervical cancers accompanied by 242 noncancer cases were collected from inhouse tissue microarray, other public RNA-seq, and microarrays. The remarkable high expression of CKS2 in cervical cancer and the ability of CKS2 overexpression to discriminate against cervical cancer and noncancer cervix tissues was revealed in most datasets (Figure 1). The overexpression of CKS2 in cervical cancer was indicated in the forest plot of SMD. The SROC curves reflected the moderate capacity of CKS2 overexpression in separating cervical cancer from noncancer cervix tissues (, ; ; Figure 6).

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3.3. Prognostic Value of CKS2 Expression for Cervical Cancer

The disease-free survival condition of cervical cancer patients (sampled from GSE44001) worsened in the group with CKS2 high expression compared to cervical cancer patients with low CKS2 expression (, ; Figure 7(c)). The prognostic results from the RNA-seq dataset were insignificant.

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3.4. The Landscape of the Genetic Mutation Types of CKS2 in Cervical Cancer

Five mRNA high cases, five with mRNA low, and one case of deep deletion were recorded in 310 cervical cancer cases from the TCGA database (Figure 8).

3.5. Diverse Functions of CKS2-Related Genes in Cervical Cancer

RNA-seq data of cervical cancer in TCGA database and 22 external microarrays (e.g., GSE7803, GSE9750, GSE46857, GSE14404, GSE29570, GSE52903, GSE52904, GSE89657, GSE39001-GPL6244, GSE27678-GPL571, GSE63678, GSE6791, GSE27678-GPL570, GSE63514, GSE4482-GPL4926, GSE138080, GSE4482-GPL3515, GSE39001-GPL201, GSE7410, GSE55940, GSE67522, and GSE26342) were subjected to differential expression analysis and correlation analysis of gene expression. One hundred and four and 335 genes were positively and negatively related to CKS2, respectively (Supplementary Table 1). The engagement of these genes in various biological events and KEGG pathways is delineated in panels of dot plots (Figures 9 and 10).

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4. Discussion

Big data produced from high-throughput RNA-seq and microarrays have been proven to be a powerful aid in oncology research, facilitating the hunting for novel biomarkers in a time-effective manner, which is how expression profiling and molecular investigations have improved the management of gynecological tumors [20–22]. Only two studies revealed the mitochondrial function of CKS2 in the aggressive development of chemo radioresistant cervical cancer and the adverse impact of CKS2 high expression on the progression-free survival of cervical cancer patients [23, 24]. However, the clinicopathological significance and molecular basis of CKS2 remain far from being expounded. Here, taking advantage of massive genetics data from multicenter microarrays and RNA-seq data, we evaluated the clinicopathological significance of CKS2 with large samples (980 cervical cancers accompanied by 422 noncancer specimens). There is one precedent in history that excavated the potential mechanisms of the tumor-boosting activities of CKS2 in cervical cancer.

Expression data from multilevels of inhouse tissue microarray, other public RNA-seq, and microarrays consistently supported the high expression of CKS2 in cervical cancer. The expression analysis results from this study were convincing because of the large sample pool containing 980 cervical cancer plus 422 noncancer specimens. This phenomenon also agrees with the findings of earlier studies [23, 24]. Furthermore, the higher expression of CKS2 in cervical cancer patients with stage II from inhouse microarrays and the adverse impact of CKS2 overexpression on the disease-free survival conditions of cervical cancer patients in GSE44001 indicated the promotive effect of CKS2 overexpression in augmenting the malignancy of cervical cancer.

After assessing the clinical significance of CKS2 in cervical cancer, we further investigated the possible mechanisms of the tumor-boosting effect of CKS2 in cervical cancer via genetic alteration analysis and functional enrichment annotation of genes co-expressed with CKS2. It could be noted from the bar chart of the alteration profile that both the mutation types of mRNA high and mRNA low appeared. Although the frequency of mRNA high and mRNA low equaled the genetic alteration profiles for the TCGA Firehose project, this only represented the mutation status of CKS2 in the RNA-seq dataset. We conjectured that there might be a predominance of mRNA high over mRNA low in large samples. This includes cervical cancer specimens from microarrays and RNA-seq datasets, which might account for the upregulation of CKS2 in cervical cancer. Apart from genetic mutation profile analysis, we also identified genes significantly related to CKS2 in cervical cancer and their functional enrichment. There was an apparent difference between the terms of biological process, molecular function, and KEGG pathways assembled by genes positively and negatively related to CKS2. At the same time, plentiful biological process terms relevant to mitotic function could be found for genes positively associated with CKS2. The terms of extracellular constituent organization emerged in biological process and molecular function terms for genes negatively related to CKS2. Variation in the functional enrichment of genes positively and negatively associated with CKS2 suggested that the interaction between CKS2 and positively or negatively coexpressed genes might influence different aspects of biological function and molecular function in the initiation and development of cervical cancer. Concerning the KEGG pathway, multiple significantly assembled pathways, including the cell cycle, spliceosome, DNA replication, cellular senescence, MAPK signaling pathway, and estrogen signaling pathway, were closely linked with the carcinogenesis and pathophysiology of cervical cancer [25–38]. In particular, the involvement of CKS2 in some significantly enriched pathways exampled by cell cycle and DNA replication has been reported by prior researchers [14, 39, 40]. Therefore, we postulated that the interrelationships between CKS2 and genes related to CKS2 might take part in cervical cancer oncogenesis through the above biological functions, molecular functions, and KEGG pathways.

The limitations of the present study were the lack of experimental validation of the functional roles of CKS2 in cervical cancer and the connections between CKS2 and other coexpressed genes, which should be warranted in future work.

5. Conclusion

In summary, CKS2 was identified as being overexpressed in CKS2 and is concerned with the clinical progression of cervical cancer. The oncogenic influence of CKS2 overexpression in cervical cancer is related to the cell cycle, DNA replication, and estrogen signaling pathways. CKS2 might serve as a valuable therapeutic target in cervical cancer.

Data Availability

The datasets generated and/or analyzed during the current study are available in the TCGA (https://portal.gdc.cancer.gov/) and GEO (https://www.ncbi.nlm.nih.gov/gds) databases.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Li Qin and Xiaoqiong Luo contributed equally to this work.

Acknowledgments

This study was financially supported by the 2019 Natural Science Foundation of Guangxi, China (No. 2019GXNSFBA245020), the High-Level Talent Scientific Research Project of the Affiliated Hospital of Youjiang Medical University for Nationalities, China (No. Y20196316), and the “139” Medical High-level Talent Training Plan and Thousands of Young and Middle-aged Backbone Teachers Cultivation Plan of Guangxi Province, China (No. 2019KY0573), and the Health and Family Planning Commission self-funded scientific research project of Guangxi Province, China (No. 220180211).

Supplementary Materials

Supplementary Table 1: genes positively and negatively related to CKS2. (Supplementary Materials)

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Copyright © 2022 Li Qin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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