Regulatory and Interacting Partners of PDLIM7 in Thyroid Cancer

Author:

Rood Kristiana123,Yamauchi Celina Romi123,Sharma Umang4,Laxa Ria T.123,Robins Collin123,Lanza Gerardo123ORCID,Sánchez-Ruiz Kidianys123,Khan Aminah123,Kim Hae Soo123,Shields Andrea5,Kennedy Kari2,Mirshahidi Saied6ORCID,Perez Mia C.25,Firek Anthony78ORCID,Munir Iqbal8,Simental Alfred A.2,Khan Salma1239ORCID

Affiliation:

1. Division of Biochemistry, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA

2. Division of Otolaryngology, Loma Linda University Health, Loma Linda, CA 92354, USA

3. Center for Health Disparities & Molecular Medicine, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA

4. School of Public Health, Loma Linda University, Loma Linda, CA 92354, USA

5. Department of Pathology & Human Anatomy, Loma Linda University School of Medicine, Loma Linda, CA 92350, USA

6. Loma Linda University Cancer Center, Loma Linda, CA 92354, USA

7. Comparative Effectiveness and Clinical Outcomes Research Center (CECORC), Riverside University Health System, 26520 Cactus Ave, Moreno Valley, CA 92555, USA

8. Department of Endocrinology, Riverside University Health System, 26520 Cactus Ave, Moreno Valley, CA 92555, USA

9. Department of Internal Medicine, Loma Linda University School of Medicine, 11085 Campus St, Loma Linda, CA 92350, USA

Abstract

Enigma protein, encoded by the PDLIM7 gene, is overexpressed in thyroid cancer in a stage-dependent manner, suggesting a potential involvement in the initiation and progression of thyroid cancer. The Enigma interacts with several cellular pathways, including PI3K/AKT, MDM2, and BMP-1. The Enigma is regulated by microRNAs. Specifically, we showed that the Enigma protein upregulation corresponds to the downregulation of Let-7 family genes. There is limited research on the interactions and regulation of the Enigma with other proteins/genes in thyroid cancer tissues, indicating a gap in current knowledge. Our aim is to establish the Enigma as a biomarker. We also aim to study the interacting partners of the Enigma signaling pathways and their probable miRNA regulation in thyroid cancer progression. Using Western blotting, densitometric analysis, immunoprecipitation (IP), and reverse IP, we detected the protein expression and protein–protein interactions in the corresponding papillary thyroid carcinomas (PTCs). Utilizing real-time qPCR assay and Pearson’s correlation test, we highlighted the correlation between PDLIM7 and Let-7g gene expression in the same tissues. The results showed the differential upregulations of the Enigma protein in different stages of PTCs compared to benign tissues along with AKT, VDR, BMP-1, and MDM2 proteins. Loss of DBP was observed in a subset of PTCs. Strong interactions of the Enigma with PI3K/AKT and MDM2 were noted, along with a weaker BMP-1 interaction. Pearson’s correlation coefficient analysis between PDLIM7 and let-7g gene expression was significant (p < 0.05); however, there was a weak inverse correlation (r = −0.27). The study suggests the potential utility of the PDLIM7-qPCR assay as a biomarker for thyroid cancer. The Enigma’s interactions with key signaling pathways may provide valuable insights into the development of thyroid cancer. The study contributes to understanding the molecular mechanisms involving the Enigma protein in thyroid cancer and highlights its potential as a biomarker.

Funder

Promote Collaborative and Translational Research, Loma Linda University School of Medicine

IMSD

Publisher

MDPI AG

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