2009
DOI: 10.1016/j.humpath.2008.07.009
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Merkel cell carcinoma expresses K homology domain–containing protein overexpressed in cancer similar to other high-grade neuroendocrine carcinomas

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Cited by 22 publications
(19 citation statements)
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“…IMP3 is expressed in malignant melanoma but not in benign nevi, even when dysplastic features are present and it is expressed in metastatic melanomas significantly more often than in early-stage melanomas [20]. In neuroendocrine carcinomas, IMP3 seems to be a marker for high-grade tumors as it is frequently found in extrapulmonary small cell carcinomas (89% positive), small cell lung carcinomas (90% positive), large cell neuroendocrine carcinomas of the lung (64% positive), and Merkel cell carcinomas (90% positive), whereas it is negative in pulmonary and extrapulmonary carcinoid tumors [21][22][23]. IMP3 is a promising new marker with high specificity and sensitivity for pancreatic adenocarcinomas in pancreatic fine needle aspirates [24,25].…”
Section: Discussionmentioning
confidence: 99%
“…IMP3 is expressed in malignant melanoma but not in benign nevi, even when dysplastic features are present and it is expressed in metastatic melanomas significantly more often than in early-stage melanomas [20]. In neuroendocrine carcinomas, IMP3 seems to be a marker for high-grade tumors as it is frequently found in extrapulmonary small cell carcinomas (89% positive), small cell lung carcinomas (90% positive), large cell neuroendocrine carcinomas of the lung (64% positive), and Merkel cell carcinomas (90% positive), whereas it is negative in pulmonary and extrapulmonary carcinoid tumors [21][22][23]. IMP3 is a promising new marker with high specificity and sensitivity for pancreatic adenocarcinomas in pancreatic fine needle aspirates [24,25].…”
Section: Discussionmentioning
confidence: 99%
“…IMP3 is considered an oncofetal protein that is expressed in fetal and carcinogenic tissue; however, the exact function of IMP3 remains unknown (7)(8)(9)(10)(11)(12). Expression of IMP3 has been studied in a wide variety of cancers, including renal cell carcinoma (13,14), adenocarcinoma of the uterine cervix (15), endometrial carcinoma (16), adenocarcinoma of the esophagus (17), malignant melanoma (18), Merkel cell carcinoma (19), urothelial carcinoma (20), neuroendocrine carcinoma of the lung (21), gastric adenocarcinoma (22), hepatocellular carcinoma (23), pancreatic (24)(25)(26)(27) and biliary tract (27) adenocarcinoma, and triple negative breast cancer (28), where this marker has frequently been associated with enhanced tumor aggressiveness and a worse outcome.…”
Section: Introductionmentioning
confidence: 99%
“…High levels of IMP3 expression have been reported to have diagnostic and/or prognostic value in different malignant tumors (kidney, ovary, liver, endometrium, esophagus, biliary tract, bladder, uterine cervix, stomach, colonrectum, esophagus, lung, exocrine pancreas, thyroid, ovary, testis, bone, and skin) [7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23][24][25] (Table 2). Our results confirmed the expression of IMP3 in the normal pituitary tissues, previously reported, using immunohistochemical, Western blotting, and RT-PCR analyses.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have shown that IMP3 is associated with aggressive and advanced carcinomas in colon, kidney, neuroendocrine skin (Merkel cell carcinoma), liver, bladder, ovary, and in soft tissue sarcomas [16][17][18][19][20][21][22][23][24][25]. On the basis of these results, IMP3 may be a useful prognostic factor in many malignant solid tumors.…”
Section: Introductionmentioning
confidence: 99%