2010
DOI: 10.2353/ajpath.2010.090402
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Primary Cell Cultures from Human Renal Cortex and Renal-Cell Carcinoma Evidence a Differential Expression of Two Spliced Isoforms of Annexin A3

Abstract: Renal-cell carcinomas (RCC) arise from the renal epithelium, account for about 85% of renal cancers, and are characterized by different subtypes having different incidences. The clear-cell (RCCcc) and papillary (RCCpap) subtypes of sporadic RCC account for about 75% and 12% of cases, respectively, and have distinct genetic abnormalities.

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Cited by 45 publications
(70 citation statements)
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“…These cultures represent a reproducible and well-characterized cellular model that maintains, in the first passages, the phenotypic and molecular characteristics of the corresponding tissue (Perego et al, 2005;Bianchi et al, 2010;Cifola et al, 2011). Our data showed that these primary cells, grown in high-glucose medium, acquired an elongated morphology but only a few molecular EMT features, and did not reach a full EMT phenotype.…”
Section: Discussionmentioning
confidence: 83%
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“…These cultures represent a reproducible and well-characterized cellular model that maintains, in the first passages, the phenotypic and molecular characteristics of the corresponding tissue (Perego et al, 2005;Bianchi et al, 2010;Cifola et al, 2011). Our data showed that these primary cells, grown in high-glucose medium, acquired an elongated morphology but only a few molecular EMT features, and did not reach a full EMT phenotype.…”
Section: Discussionmentioning
confidence: 83%
“…Immunofluorescence and stress fiber analysis Cells were seeded on glass coverslips, fixed and incubated with the indicated primary antibodies and, when necessary, with secondary antibodies (Table S1), as previously described (Bianchi et al, 2010). Stress fibers were labeled by Alexa-Fluor-594-phalloidin (dilution 1:100; Molecular Probes, Carlsberg, CA).…”
Section: Human Primary Tubular Cell Cultures and Treatmentsmentioning
confidence: 99%
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“…Annexin A3 may act as a tumor suppressor or tumor promoter depending upon the type of tumor cell and tissue. Annexin A3 has been shown to be upregulated [13] in prostate cancer, and downregulated in kidney and thyroid cancers [14,15]. Increased expression of Annexin A3 enhanced the drug resistance of ovarian and liver cancers [16,19], promoted the progression of pancreatic, rectal, and glandular cancers [17], and accelerated the metastasis of lung cancer [18].…”
mentioning
confidence: 99%