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Determination of Protein Expression Level in Cultured Cells by Immunocytochemistry on Paraffin-embedded Cell Blocks
Published on: May 20, 2018
Expression of calcyclin-binding protein/Siah-1 interacting protein in normal and malignant human tissues: an
Huihong Zhai1, Yongquan Shi, Haifeng Jin
1State Key Laboratory of Cancer Biology, Institute of Digestive Diseases, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Abstract:
Calcyclin-binding protein (CacyBP)/Siah-1 interacting protein (SIP), a component of ubiquitin-mediated proteolysis, could bind the Skp1-Cul1-F box protein complex. Although CacyBP/SIP was implicated in p53-induced beta-catenin degradation, its exact function was still unknown. Our previous studies showed that CacyBP/SIP could modulate the multidrug-resistant phenotype of gastric cancer cells and was highly expressed in gastric cancer tissues compared with that in non-cancerous tissues. In this study, CacyBP/SIP protein expression profile in a broad range of human normal tissues and carcinomas was analyzed by immunohistochemistry staining with anti-CacyBP/SIP monoclonal antibody first produced in our laboratory. CacyBP/SIP was generally localized in the cytoplasm/nucleus. Positive staining of CacyBP/SIP was found in brain, heart, lymph node, and esophagus. Weak staining was shown in the rectum and kidney. No CacyBP/SIP was detected in other normal tissues. However, CacyBP/SIP was ubiquitously detected in all kinds of tumor tissues and was highly expressed in nasopharyngeal carcinoma, osteogenic sarcoma, and pancreatic cancer. To our knowledge, this is the first study on the CacyBP/SIP expression pattern in a broad range of human normal and tumor tissues. The data presented should serve as a useful reference for other investigators in future studies of CacyBP/SIP functions. Hopefully, this knowledge will lead to discovery of more roles of CacyBP/SIP in tumorigenesis.
Insights
Calcyclin-binding protein (CacyBP)/Siah-1 interacting protein (SIP) is highly expressed in various cancers. This study maps CacyBP/SIP expression in normal and tumor tissues, revealing its ubiquitous presence in tumors and potential role in tumorigenesis.
Area of Science:
- Molecular Biology
- Cancer Research
- Proteomics
Background:
- Calcyclin-binding protein (CacyBP)/Siah-1 interacting protein (SIP) is involved in ubiquitin-mediated proteolysis and has been linked to beta-catenin degradation.
- Previous research indicated CacyBP/SIP modulates multidrug resistance in gastric cancer and is upregulated in these tissues.
Purpose of the Study:
- To comprehensively analyze the protein expression profile of CacyBP/SIP across a wide spectrum of human normal tissues and carcinomas.
- To establish a baseline understanding of CacyBP/SIP expression patterns for future functional studies in tumorigenesis.
Main Methods:
- Immunohistochemistry staining using a newly developed anti-CacyBP/SIP monoclonal antibody.
- Analysis of CacyBP/SIP protein localization (cytoplasm/nucleus) and expression levels in diverse human tissues and cancer types.
Main Results:
- CacyBP/SIP exhibited positive staining in brain, heart, lymph node, and esophagus, with weak staining in the rectum and kidney; it was undetectable in most other normal tissues.
- In contrast, CacyBP/SIP was ubiquitously detected in all analyzed tumor tissues.
- Notably high expression levels of CacyBP/SIP were observed in nasopharyngeal carcinoma, osteogenic sarcoma, and pancreatic cancer.
Conclusions:
- This study presents the first extensive analysis of CacyBP/SIP expression in human normal and tumor tissues.
- The findings highlight CacyBP/SIP as a potential pan-cancer marker with significantly elevated expression in numerous malignancies.
- This expression data provides a crucial reference for future research into the functional roles of CacyBP/SIP in cancer development.
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