Abstract. The AC3-33 gene encodes a secretory protein that can inhibit Elk1 transcriptional activity via the ERK1/2 pathway. In the current study, in situ RNA hybridization was used to detect the AC3-33 gene expression in multiple organ cancer and cancer-adjacent normal tissue. The results showed that the expression level of AC3-33 varies across different tissues. AC3-33 exhibited positive expression in squamous cell carcinoma of the esophagus, adenocarcinoma of the rectum, hepatocellular carcinoma, squamous cell carcinoma (SCC) of the lung, cancer-adjacent normal hepatic tissue, clear cell carcinoma of the kidney, invasive ductal carcinoma of the breast, SCC of the uterine cervix and cancer-adjacent normal kidney tissue. Negative expression of AC3-33 was observed in adenocarcinoma of the stomach and colon, cancer-adjacent normal esophageal tissue, cancer-adjacent normal gastric tissue, cancer-adjacent normal colon tissue, cancer-adjacent normal rectal tissue, serous adenocarcinoma of the ovary and cancer-adjacent normal ovarian tissue. However, the expression of AC3-33 in cancer adjacent normal breast tissue was partially positive. In conclusion, the AC3-33 gene does exhibit positive expression in certain carcinomas, which may indicate that AC3-33 has a significant involvement in the development and progression of these carcinomas.
IntroductionAC3-33 (GenBank name: C3orf33, accession no. FLJ31139), also known as chromosome 3 open reading frame 33, encodes a classical secretory protein with a predicted molecular mass of 29.3 kDa (1). Transcription factor activator protein-1 (AP-1) is crucial in the regulation of cellular proliferation, transformation and death (2). Using a dual-luciferase reporter assay system, our previous study found that significantly inhibited AP-1 transcriptional activity. Further investigation indicated that AC3-33 significantly inhibited the transcriptional activity of Elk1 and c-jun, but not of c-fos; additionally, AC3-33 significantly inhibits Elk1 transcriptional activity via the extracellular-signal-regulated kinases 1/2/mitogen-activated protein kinases pathway. This occurs via disruption of ERK1/2 MAPK pathway (3). AC3-33 is highly expressed in a number of tissues, including the adrenal glands and cervix, and expression is comparatively significantly reduced in the human leukemia cell lines, K562 and KG1a (4). However, the expression of AC3-33 in multiple organ tumors and cancer-adjacent normal tissue remains to be elucidated.In the present study, RNA in situ hybridization was used to detect the AC3-33 gene expression in multiple organ tumors and cancer-adjacent normal tissue. An improved understanding of the expression of AC3-33 may offer more information as to the role of AC3-33 in the pathological process of tumorigenesis, which may subsequently provide a new insight into AC3-33 and its potential applications in the treatment and diagnosis of human disease.
Materials and methodsTissue microarray. Tissue microarray was purchased from Chaoying Biotechnology (Xian, China; MCN602). ...