2000
DOI: 10.1136/jcp.53.8.626
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Differential expression of CD34 in normal colorectal tissue, peritumoral inflammatory tissue, and tumour stroma

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Cited by 70 publications
(76 citation statements)
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“…Also, Kuroda et al (2004) studied the CD34-positive cells diffusion in intestinal tumors and concluded that stromal cells of CD34-positive, present in the area between sub-mucosal and sub-serous of normal tissue, were removed from this region after tumor invasion and were transferred to deeper layers of tumors. The results were confirmed in another study that showed the inflamed tissue in tumor margins and tumor stroma of stromal cells are free of CD34 (Nakayama et al, 2000).…”
Section: Discussionsupporting
confidence: 74%
See 1 more Smart Citation
“…Also, Kuroda et al (2004) studied the CD34-positive cells diffusion in intestinal tumors and concluded that stromal cells of CD34-positive, present in the area between sub-mucosal and sub-serous of normal tissue, were removed from this region after tumor invasion and were transferred to deeper layers of tumors. The results were confirmed in another study that showed the inflamed tissue in tumor margins and tumor stroma of stromal cells are free of CD34 (Nakayama et al, 2000).…”
Section: Discussionsupporting
confidence: 74%
“…In moderately differentiated tumors, CD34 expression was significantly lower than less differentiated cancers and CD34 expression in diffuse type was more than intestinal one. Similar results were reported on the positive relationship between this marker and differentiation and tumor type on the intestinal adenocarcinoma in numerous studies (Choi et al, 2009;Feng et al, 2010;Nakayama et al, 2000). Although, the depth of invasion was not significantly different from marker expression but the difference was too much, so that 87.5% of positive cases had a depth of T3 that of all tumors in depth of T3, a quarter of them have expressed a marker.…”
Section: Discussionsupporting
confidence: 72%
“…+ fibrocytes (CD34 is a 110 kDa surface antigen selectively expressed on human haematopoietic progenitor cells) originating from myeloid precursors in the bone marrow were considered as a source of myofibroblasts in cancer of the colon [129], pancreas, [130], and breast [131]. Experimental studies have shown that CD34 + fibrocytes are attracted by the secondary lymphoid chemokine CCL-21, a ligand of the CCR7 chemokine receptor, and invade sites of tissue damage in vivo.…”
Section: The Origin Of Myofibroblastsmentioning
confidence: 99%
“…They added that using CD34 immunohistochemistry may be useful in detecting large neoplasms. In another study, it was shown that most stromal cells are CD34+in the sub-mucosal, muscularis propria and suborosa as well as normal perirectal tissues, while the inflamed tissues around tumor and tumor stroma of stromal cells lacked CD34 (Nakayama et al, 2000). The study findings showed that lack of CD34 expression of stromal cells in colorectal adenocarcinoma is involved in creation of a desmoplastic reaction.…”
Section: Discussionmentioning
confidence: 76%
“…Another study examined the immunohistochemical analysis of CD34 in colorectal cancer, colorectal adenomas and colorectal non-neoplastic lesions. In this study, the expression of CD34 was associated with recurrence, metastasis and survival of colorectal malignancies and this indicated the prognostic role of CD34 in colorectal cancer (Nakayama et al, 2000). Liang et al (2004) used the immunohistochemical expression of CD34 as a marker for the diagnosis and assessment of MicroVessel Density (MVD) and its association with the capillary development in colon cancer cells.…”
Section: Discussionmentioning
confidence: 99%