X Liu1, L Ye, J Wang, D Fan. 1. Institute of Digestive Disease, Xi Jing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Abstract
OBJECTIVE: To examine the expression of heat shock protein (HSP) 90 beta in human gastric cancer tissue and SGC7901/VCR of MDR-type gastric cancer cell line. METHODS: Immunohistochemical staining and in situ hybridization methods. RESULTS: Heat shock protein 90 beta was mainly located in the cell cytoplasma and weakly expressed in non-cancerous gastric mucosa. The expression rates of HSP90 beta in normal gastric mucosa, gastritis and paracancer tissues were 11.76%, 13.04% and 11.42% respectively, and there were no significant differences between them (P > 0.05). The expression of HSP90 beta was increased in gastric cancer. The positive rate of HSP90 beta in gastric cancer tissue was 30.00%, and was higher than non-cancerous gastric mucosa (P < 0.05). The expression rates of HSP90 beta in well differentiated, moderately differentiated, poorly differentiated gastric cancer and mucinous carcinoma were 15.38%, 31.25%, 33.33%, and 42.85% respectively. The expression of HSP90 beta in SGC7901/VCR of MDR-type gastric cell line was higher than in its parental cell line SGC7901. In situ hybridization showed that the positive signal of HSP90 beta was mainly located in the cell cytoplasma. CONCLUSIONS: The expression of HSP90 beta was higher in gastric cancer tissue than in non-cancerous gastric mucosa. In gastric cancer tissue, the expression of HSP90 beta was greater in poorly differentiated cancer tissue, and in SGC7901/VCR of MDR-type gastric cancer cell line the expression of HSP90 beta was higher than that in its parental cell line SGC7901.
OBJECTIVE: To examine the expression of heat shock protein (HSP) 90 beta in humangastric cancer tissue and SGC7901/VCR of MDR-type gastric cancer cell line. METHODS: Immunohistochemical staining and in situ hybridization methods. RESULTS: Heat shock protein 90 beta was mainly located in the cell cytoplasma and weakly expressed in non-cancerous gastric mucosa. The expression rates of HSP90 beta in normal gastric mucosa, gastritis and paracancer tissues were 11.76%, 13.04% and 11.42% respectively, and there were no significant differences between them (P > 0.05). The expression of HSP90 beta was increased in gastric cancer. The positive rate of HSP90 beta in gastric cancer tissue was 30.00%, and was higher than non-cancerous gastric mucosa (P < 0.05). The expression rates of HSP90 beta in well differentiated, moderately differentiated, poorly differentiated gastric cancer and mucinous carcinoma were 15.38%, 31.25%, 33.33%, and 42.85% respectively. The expression of HSP90 beta in SGC7901/VCR of MDR-type gastric cell line was higher than in its parental cell line SGC7901. In situ hybridization showed that the positive signal of HSP90 beta was mainly located in the cell cytoplasma. CONCLUSIONS: The expression of HSP90 beta was higher in gastric cancer tissue than in non-cancerous gastric mucosa. In gastric cancer tissue, the expression of HSP90 beta was greater in poorly differentiated cancer tissue, and in SGC7901/VCR of MDR-type gastric cancer cell line the expression of HSP90 beta was higher than that in its parental cell line SGC7901.
Authors: Thomas R Cawthorn; Juan C Moreno; Moyez Dharsee; Danh Tran-Thanh; Suzanne Ackloo; Pei Hong Zhu; Girish Sardana; Jian Chen; Peter Kupchak; Lindsay M Jacks; Naomi A Miller; Bruce J Youngson; Vladimir Iakovlev; Cynthia J Guidos; Katherine A Vallis; Kenneth R Evans; David McCready; Wey L Leong; Susan J Done Journal: PLoS One Date: 2012-02-20 Impact factor: 3.240
Authors: X Wu; A Wanders; P Wardega; B Tinge; L Gedda; S Bergstrom; L Sooman; J Gullbo; M Bergqvist; P Hesselius; J Lennartsson; S Ekman Journal: Br J Cancer Date: 2009-01-13 Impact factor: 7.640