2009
DOI: 10.1016/j.canlet.2008.10.019
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Proteomic identification of tumor-associated protein in ovarian serous cystadenocarinoma

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Cited by 19 publications
(18 citation statements)
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“…Despite the relatively small number of tissue and ascites specimens studied, the majority of proteins identified in the present study as being significantly differentially secreted from malignant and CTRL cell samples had been detected in previous studies (8)(9)(10)(11)(12)(13)(14)(15)(16), confirming their potent and important role. To the best of our knowledge, proteins including HSP-10 and DKK3, had not previously been identified by a proteomic approach, but had been suggested as potent markers using alternate approaches (19,30); however the present study was unable to confirm their utility as biomarkers of serous ovarian cancer by the immunological method.…”
Section: Discussionsupporting
confidence: 76%
See 1 more Smart Citation
“…Despite the relatively small number of tissue and ascites specimens studied, the majority of proteins identified in the present study as being significantly differentially secreted from malignant and CTRL cell samples had been detected in previous studies (8)(9)(10)(11)(12)(13)(14)(15)(16), confirming their potent and important role. To the best of our knowledge, proteins including HSP-10 and DKK3, had not previously been identified by a proteomic approach, but had been suggested as potent markers using alternate approaches (19,30); however the present study was unable to confirm their utility as biomarkers of serous ovarian cancer by the immunological method.…”
Section: Discussionsupporting
confidence: 76%
“…Certain previous studies have analyzed the proteomic profiles of ovarian tumor tissues, cell lines, urine, ascites fluid and blood samples (8)(9)(10)(11)(12)(13)(14). Analysis of the ovarian cancer cell line secretome has also provided information on potential markers (11,15).…”
Section: Introductionmentioning
confidence: 99%
“…PRDX3 is an active responder to oxidative stress, and its expression of concordantly augmented to remove cellular ROS and inhibit apoptosis, which is beneficial to cancer growth and invasion. Furthermore, short hairpin RNA (shRNA)-mediated loss in functional PRDX3 expression led to significant suppression of migration and transendothelial invasion in MCF-7 breast cancer cells in vitro and significant inhibition of breast cancer metastasis in vivo (Kim et al, 2009;Li et al, 2009;Liu et al, 2010;Wu et al, 2010). Recently, abundant evidence has also confirmed that tissue-specific expression of PRDX3 plays an important role in hepatocarcinoma progression (Dai et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, the overexpression of PRDX3 had also been found in cervical cancer, colorectal cancer and ovarian serous cystadenocarinoma. (25,28,29). However, there are few reports on the relationship between PRDX3 and the progression of HCC, and thus, we focused on the study of thioredoxin-dependent peroxide reductase PRDX3.…”
Section: Discussionmentioning
confidence: 99%