2008
DOI: 10.1016/j.humpath.2007.12.012
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Expression of RNA-binding protein IMP3 (KOC) in benign urothelium and urothelial tumors

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Cited by 39 publications
(44 citation statements)
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References 30 publications
(49 reference statements)
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“…a disturbance in the cell cycle control mechanism following Dna methyl transferase i upregulation and defects in the p53 and rb pathways are accused of playing a role in the development of invasive tumors (3,6). Missense mutations found in the p53 tumor suppressor gene have been detected in approximately 50% of bladder tumors with an unfavorable prognosis (1,4).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…a disturbance in the cell cycle control mechanism following Dna methyl transferase i upregulation and defects in the p53 and rb pathways are accused of playing a role in the development of invasive tumors (3,6). Missense mutations found in the p53 tumor suppressor gene have been detected in approximately 50% of bladder tumors with an unfavorable prognosis (1,4).…”
Section: Discussionmentioning
confidence: 99%
“…Superficial tumors are quite benign while a high mortality rate has been reported with invasive tumors. The histopathological stage and grade are therefore the two most important factors in determining the behavior and treatment plan for bladder tumors (2,3). However, Ta ve T1 tumors can exhibit different biological behavior (4).…”
Section: Anahtar Sözcükler: Mesane üRotelyal Karsinom Imp3 Transismentioning
confidence: 99%
“…10 Later, KOC was shown to be identical to IMP3 and L523S proteins. 8,11 In the present study, we investigated the correlation among expression of IMP3, clinicopathologic characteristics, and prognosis, in patients with OSCC.…”
Section: Introductionmentioning
confidence: 99%
“…After embryogenesis and development, IMP3 expression is detectable in occasional adult tissues, including the internal root sheath of hair follicles, germinal centers of lymph nodes ( Figure 1B), patchy gastrointestinal tract and bronchiolar epithelium (Righi, Zhang et al;Mueller-Pillasch, Pohl et al 1999;Nielsen, Christiansen et al 1999;Hammer, Hansen et al 2005;Simon, Bourne et al 2007;Xu, Bourne et al 2007;Mentrikoski, Ma et al 2009). In addition to its expression in fetal development, IMP3 has been detected in numerous malignancies including germ cell carcinomas, renal cell carcinoma, small and non-small cell lung carcinomas, urothelial carcinoma, endometrial serous and cervical carcinomas, Merkel cell carcinoma, extrapulmonary small cell carcinoma, various lymphomas, thyroid carcinoma, mammary breast carcinoma, colonic, gastric and esophageal adenocarcinomas, and osteogenic sarcoma (Asioli, Erickson et al ;Findeis-Hosey, Yang et al ;Jin, Seys et al ;Righi, Zhang et al ;Wang, Fan et al 2003;Hammer, Hansen et al 2005;Jiang 2007;Li, Rock et al 2007;Simon, Bourne et al 2007;Do, Kim et al 2008;Li, Xu et al 2008;Pryor, Bourne et al 2008;Zheng, Yi et al 2008;Jeng, Wang et al 2009;King, Pasha et al 2009;Li, Yan et al 2009;Li, Huang et al 2009;Lu, Vohra et al 2009;Mentrikoski, Ma et al 2009;Pryor, Simon et al 2009;Slosar, Vohra et al 2009;Walter, Prasad et al 2009;Yuan, Wang et al 2009). Moreover, IMP3 expression has been shown to be a marker of poorer prognosis with decreased overall survival in several tumors including renal cell carcinoma, mammary breast carcinoma, non-small cell lung carcinoma, and numerous gastrointes...…”
mentioning
confidence: 99%