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RhCG is downregulated in oesophageal squamous cell carcinomas, but expressed in multiple squamous epithelia
Bao-Sheng Chen1, Zhi-Xiong Xu, Xin Xu
1National Laboratory of Molecular Oncology, Cancer Institute, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Abstract:
To better understand the molecular events underlying the development of oesophageal cancer, we have isolated the genes dysregulated in primary oesophageal cancer tissues using a modified differential display polymerase chain reaction (DD-PCR). In the present study, a gene designated C15orf6 was identified. The C15orf6 gene, encompassing 25 kb, is composed of 11 exons with a mRNA of 1948 bp. Database searching showed that C15orf6 was 100% homologous to the Rh type C-glycoprotein (RhCG) with the same open reading frame, but 16 bp longer than RhCG at the 5'-end. The gene was highly expressed in human oesophagus, cervix, oral cavity, skin and kidney, but undetectable in the other 14 adult normal tissues examined. Northern blot, RT-PCR and western blot analysis showed that RhCG/C15orf6 was frequently lost or dramatically reduced in primary oesophageal cancer tissues (30/34) compared with the corresponding normal oesophageal mucosa. Three oesophageal-cancer cell lines tested lacked RhCG/C15orf6 expression. Immunohistochemistry revealed that in normal oesophageal tissues, RhCG/C15orf6 was mainly expressed in the plasma membrane of the epithelial cells. In addition, Rh-associated glycoprotein (RhAG) expression was also commonly silenced in both oesophageal cancer cell lines (2/3) and primary oesophageal cancer tissues (11/13). To our knowledge, this is the first time that RhAG expression has been seen in oesophageal epithelium and extends the functional role of the RhAG protein beyond the erythrocyte. These data suggest that inactivation of RhCG/C15orf6 and RhAG occurs frequently during the development of human oesophageal cancer.
Insights
The Rh type C-glycoprotein (RhCG) and Rh-associated glycoprotein (RhAG) are frequently lost or reduced in oesophageal cancer tissues. This suggests their inactivation plays a role in oesophageal cancer development.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Oesophageal cancer development involves complex molecular events.
- Understanding gene dysregulation is crucial for identifying cancer mechanisms.
Purpose of the Study:
- To identify genes dysregulated in oesophageal cancer.
- To investigate the role of Rh type C-glycoprotein (RhCG) and Rh-associated glycoprotein (RhAG) in oesophageal cancer.
Main Methods:
- Modified differential display polymerase chain reaction (DD-PCR) to isolate dysregulated genes.
- Northern blot, RT-PCR, and western blot to analyze gene expression.
- Immunohistochemistry to determine protein localization.
Main Results:
- The RhCG/C15orf6 gene was identified and found to be homologous to RhCG.
- RhCG/C15orf6 expression was significantly reduced or lost in 30/34 primary oesophageal cancer tissues.
- RhAG expression was also commonly silenced in oesophageal cancer tissues and cell lines.
Conclusions:
- Inactivation of RhCG/C15orf6 and RhAG is frequent in oesophageal cancer development.
- This study reveals a novel role for RhAG in oesophageal epithelium beyond its known function in erythrocytes.