Background: Invasion and metastasis are two characteristics of malignant tumors, which perform by proteolytic destruction of the components of basement membrane (BM) and cell migration. The aim of this study was to evaluate the immunohistochemical (IHC) assessment of type IV collagen and laminin-332 γ2 (Ln-332 γ2) chain expression in well-differentiated oral squamous cell carcinoma (OSCC) and oral verrucous carcinoma (OVC), because these two lesions have same histopathologic findings whereas they have different biological behaviors.
Methods: Destruction of BM and cell migration were evaluated by IHC in 15 cases of epithelial hyperplasia with no dysplasia (A group), 15 cases of OVC (B group) and 15 cases of well-differentiated OSCC (C group).
Results: There was a significant difference in type IV collagen immunohistochemical staining between three groups, but there were no significant differences between B and C groups. Expression of Ln-332 γ2 chain was not detected in A group. Ln-332 γ2 chain labeling index had significantly difference between B and C groups. The number of Ln-332 γ2 chain immunostaining positive cells was less than 5% in B group and over than 5% in C group which there were significantly differences between these two groups.
Conclusions: Isolated immunohistochemical study of type IV collagen does not clearly define that a lesion is invasive or non-invasive and evaluation of Ln-332 γ2 chain expression (cut-off 5%) may be useful as a marker for description of biological differences and diagnosis of OVC from well-differentiated OSCC, especially in doubtful cases.
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http://dx.doi.org/10.1111/j.1600-0714.2010.00983.x | DOI Listing |
Zhongguo Yi Miao He Mian Yi
June 2009
Affiliated Hospital of Beihua University, Jilin 132000, Jilin, China.
Objective: To study genetic characteristic of fusion gene (F gene) of wild type measles virus circulated in 2006, analysis the variation regular of F gene through comparing with measles virus of 1999-2003.
Method: 9 representative strains, which isolated from 8 provinces in 2006, were selected. The whole F gene were amplified by reverse transcript-polymerase chain reaction and were sequenced, then they were compared with the nucleotide acid sequences of Chinese measles vaccine strains and the representative strains of 1999-2003, finally the phylogenetic analysis were conducted.
Zhongguo Yi Miao He Mian Yi
February 2009
State Key Laboratory for Molecuar Virology and Genetic Engineering, Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Preverntion, Beijing 100050, China.
Objective: To study genetic characteristics of fusion gene (F gene) of H1 genotype of wild measles virus circulated in China from 1999 to 2003.
Method: 13 H1 genotype representative strains including 8 subgenotype H1a strains and 5 subgenotype H1b strains isolated in mainland China during 1999-2003 were selected. Entire F gene were amplified by reverse transcript-polymerase chain reaction and sequenced, then they were compared with the nucleotide acid sequences of Chinese measles vaccine strains and the representative strains of A, D3, D6, D7 and E genotypes from other countries.
Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao (Shanghai)
January 1998
Shanghai Institute of Biochemistry, the Chinese Academy of Sciences, Shanghai 200031, China.
By using site-directed mutagenesis, we created a unique Xho I site in the CDR3 of the heavy-chain variable domain (V(H)). Two antibody molecules, one carrying one or and the other two repeats of an immunodominant epitope AA32-45 (GVYLLPRRGPRLGV) of the hepatitis C virus core protein in CDR3 of V(H) were engineered and designated Ig-E1, Ig-E2 respectively. We found that both antigenized antibodies lost the HBsAg-binding ability and the insertion of one repeat of GVYLLPRRGPRLGV epitope into the CDR3 of the V(H) domain did not appreciably affect the H chain to assemble with L chain to form a stable H(2)L(2) tetramer.
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