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Expression of HuR and Cyclooxygenase-2 in Nodular Fasciitis and Low-Grade Sarcoma: An Immunohistochemical Study. HuR和环氧合酶-2在结节性筋膜炎和低级别肉瘤中的表达:免疫组织化学研究。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.270
Hyun-Jin Son, Tae-Hwa Baek, Seung Yun Lee, Joo-Heon Kim, Dong-Wook Kang, Hye-Kyung Lee, Mee-Ja Park

Background: Nodular fasciitis is the most common reactive mesenchymal lesion to be misidentified as a type of sarcoma. HuR is an mRNA-binding protein that can stabilize cyclooxygenase-2 (COX-2) mRNA leading to COX-2 overexpression. The aim of this study is a comparison of the expressions of COX-2 and HuR and the relationships between their expressions and the clinicopathological parameters in nodular fasciitis and low-grade sarcoma.

Methods: We measured the expression of HuR and COX-2 in 21 cases of nodular fasciitis and 37 cases of low-grade sarcoma using immunohistochemistry.

Results: The frequency of cytoplasmic immunoreactivity for HuR was 5 of 21 cases of nodular fasciitis (23.8%) and 23 of 37 cases of low-grade sarcoma (62.1%) (p=.013). COX-2 expression was moderate or strong in nodular fasciitis (12/21, 57.1%) and in low-grade sarcoma (29/37, 78.4%) (p=.034). In addition, a significant difference existed between these two entities in terms of the relationship between moderate or strong COX-2 expression and HuR cytoplasmic immunoreactivity (p=.009). Moderate or strong COX-2 immunoreactivity correlated with nuclear (p=.016) or cytoplasmic HuR (p=.024) expression in low-grade sarcoma but not in nodular fasciitis.

Conclusions: This study suggests that HuR and COX-2 expression may be useful to differentiate nodular fasciitis from low-grade sarcoma.

背景:结节性筋膜炎是最常被误诊为肉瘤的反应性间质病变。HuR是一种mRNA结合蛋白,可以稳定环氧合酶-2 (COX-2) mRNA,导致COX-2过表达。本研究的目的是比较结节性筋膜炎和低级别肉瘤中COX-2和HuR的表达及其与临床病理参数的关系。方法:应用免疫组化方法检测21例结节性筋膜炎和37例低级别肉瘤中HuR和COX-2的表达。结果:21例结节性筋膜炎患者中有5例出现细胞质免疫反应(23.8%),37例低级别肉瘤患者中有23例出现细胞质免疫反应(62.1%)(p= 0.013)。COX-2在结节性筋膜炎(12/21,57.1%)和低级别肉瘤(29/37,78.4%)中表达中等或强烈(p= 0.034)。此外,在中度或强烈COX-2表达与HuR细胞质免疫反应性的关系方面,两种实体存在显著差异(p= 0.009)。中度或强烈的COX-2免疫反应性与低级别肉瘤的核表达(p= 0.016)或细胞质HuR (p= 0.024)相关,但与结节性筋膜炎无关。结论:本研究提示HuR和COX-2的表达可能有助于区分结节性筋膜炎和低级别肉瘤。
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引用次数: 1
The clinicopathological significance of epithelial mesenchymal transition associated protein expression in head and neck squamous cell carcinoma. 头颈部鳞状细胞癌上皮间充质转化相关蛋白表达的临床病理意义。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.263
Kyu Ho Kim, Lucia Kim, Suk Jin Choi, Jee Young Han, Joon Mee Kim, Young Chae Chu, Young-Mo Kim, In Suh Park, Joo Han Lim

Background: Epithelial mesenchymal transition (EMT) has an important role in invasion and metastasis of tumor cells. The purpose of this study was to evaluate the roles of EMT-associated proteins on progression and metastasis as a prognostic/predictive factor in curatively-resected (R0) head and neck squamous cell carcinoma (HNSCC).

Methods: A total of 118 patients who received curative surgery for HNSCC at Inha University Hospital between January 1996 and December 2011 were included. We used protein immunohistochemistry to evaluate the expression of E-cadherin, vimentin, and EZH2 on tissue microarrays. Also, we reviewed all medical records and analyzed the relationship between the expression of EMT-associated proteins and prognosis.

Results: The E-cadherin-negative group showed more moderate/poor differentiation of cancer cell type than the higher E-cadherin-expressing group (p=.016) and high EZH2 expression was significantly correlated with nodal metastasis (p=.012). Our results demonstrate a significant association between high expression of EZH2 and vimentin and presence of distant progression (p=.026). However, expression of E-cadherin, vimentin, and EZH2 was not significantly associated with overall survival.

Conclusions: These findings suggest that an EMT-associated protein expression profile is correlated with aggressiveness of disease and prognosis, and could be a useful marker for determination of additional treatment in curatively-resected HNSCC patients.

背景:上皮间充质转化(Epithelial mesenchymal transition, EMT)在肿瘤细胞的侵袭和转移中起重要作用。本研究的目的是评估emt相关蛋白作为治疗性切除(R0)头颈部鳞状细胞癌(HNSCC)的预后/预测因素在进展和转移中的作用。方法:选取1996年1月至2011年12月在仁荷大学附属医院接受根治性手术治疗的HNSCC患者118例。我们使用蛋白免疫组化技术评估E-cadherin、vimentin和EZH2在组织芯片上的表达。此外,我们回顾了所有的医疗记录,并分析了emt相关蛋白的表达与预后的关系。结果:e -cadherin阴性组与e -cadherin高表达组相比,中差分化程度更高(p= 0.016), EZH2高表达与淋巴结转移有显著相关性(p= 0.012)。我们的研究结果表明,EZH2和vimentin的高表达与远处进展之间存在显著关联(p= 0.026)。然而,E-cadherin、vimentin和EZH2的表达与总生存率无显著相关性。结论:这些发现表明,emt相关蛋白表达谱与疾病的侵袭性和预后相关,可能是确定治愈性切除的HNSCC患者是否需要额外治疗的有用标记。
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引用次数: 16
Differential Features of Microsatellite-Unstable Colorectal Carcinomas Depending on EPCAM Expression Status. 微卫星-不稳定型结直肠癌EPCAM表达状态的差异特征
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.276
Jung Ho Kim, Jeong Mo Bae, Kyung-Ju Kim, Ye-Young Rhee, Younghoon Kim, Nam-Yun Cho, Hye Seung Lee, Mee Soo Chang, Gyeong Hoon Kang

Background: Recent studies have revealed that a small subset of Lynch syndrome-associated colorectal carcinomas (CRCs) is caused by a germline EPCAM deletion-induced MSH2 epimutation. Based on the finding of this genetic alteration, we investigated the implications of EPCAM expression changes in microsatellite instability-high (MSI-H) CRCs.

Methods: Expression of EPCAM and DNA mismatch repair proteins was assessed by immunohistochemistry in 168 MSI-H CRCs. Using DNA samples of these tumors, MLH1 promoter methylation status was also determined by methylation-specific real-time polymerase chain reaction method (MethyLight).

Results: Among 168 MSI-H CRCs, complete loss (CL) and focal loss (FL) of EPCAM expression was observed in two (1.2%) and 22 (13.1%) cases, respectively. Both of the EPCAM-CL cases were found in MSH2-negative tumors without MLH1 promoter methylation. However, only nine of the 22 EPCAM-FL tumors had MSH2 deficiency. Of the 22 EPCAM-FL tumors, 13 showed MLH1 loss, and among them, nine cases were determined to have MLH1 methylation. EPCAM-FL was significantly associated with advanced stage (p=.043), distant metastasis (p=.003), poor differentiation (p=.001), and signet ring cell component (p=.004).

Conclusions: Loss of EPCAM expression is differentially associated with clinicopathological and molecular features, depending on the completeness of the loss, in MSI-H CRCs.

背景:最近的研究表明,一小部分Lynch综合征相关结直肠癌(crc)是由种系EPCAM缺失诱导的MSH2上皮化引起的。基于这一基因改变的发现,我们研究了EPCAM表达变化在微卫星不稳定性高(MSI-H) crc中的意义。方法:采用免疫组化方法检测168例MSI-H细胞EPCAM和DNA错配修复蛋白的表达。使用这些肿瘤的DNA样本,MLH1启动子的甲基化状态也通过甲基化特异性实时聚合酶链反应方法(MethyLight)来确定。结果:168例MSI-H crc中,EPCAM表达完全缺失(CL) 2例(1.2%),局灶性缺失(FL) 22例(13.1%)。EPCAM-CL病例均出现在msh2阴性肿瘤中,且MLH1启动子未甲基化。然而,22例EPCAM-FL肿瘤中只有9例存在MSH2缺陷。22例EPCAM-FL肿瘤中,13例MLH1缺失,其中9例MLH1甲基化。EPCAM-FL与晚期(p= 0.043)、远处转移(p= 0.003)、分化差(p= 0.001)和印戒细胞成分(p= 0.004)显著相关。结论:在MSI-H crc中,EPCAM表达的缺失与临床病理和分子特征有不同的相关性,这取决于缺失的完整性。
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引用次数: 16
Solitary myofibroma of the adult mandible: a case report and review of literature. 成人下颌骨孤立性肌纤维瘤1例报告及文献复习。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.307
Yong-Moon Lee, Seung-Myoung Son, Kyoung Won Kim, Ok-Jun Lee
Myofibroma is a rare benign neoplasm of myofibroblastic cells that can occur in either a solitary or multicentric form. Both forms were described as infantile myofibromatosis because of its multiplicity, typical age distribution (first decade of life), and frequent involvement of deep structures, including the central nervous system and visceral organs such as lung, heart, gastrointestinal tract, liver, kidney, and pancreas. 1 In contrast to the multicentric form, solitary myofibroma usually presents as a cu taneous or subcutaneous mass of the head and neck region. 2 In
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引用次数: 12
Recurrent thyroid papillary carcinoma in children under ten years old: report of two cases and literature review. 10岁以下儿童复发性甲状腺乳头状癌2例报告并文献复习。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.297
Byeong-Joo Noh, Ji-Youn Sung, Youn-Wha Kim, Yong-Koo Park

Papillary thyroid carcinoma (PTC) in children under ten years old is very rare. To date, 18 cases of PTC in children under ten years old (including our two cases) have been reported in Korea. Here, we describe two cases of recurrent PTC with follicular variant and conventional type in an 8-year-old boy and a 7-year-old boy, respectively, and discuss clinicopathologic and molecular characteristics that differ in pediatric patients from adults.

甲状腺乳头状癌(PTC)在十岁以下的儿童是非常罕见的。迄今为止,韩国已报告了18例10岁以下儿童PTC(包括我们的2例)。在这里,我们分别描述了两例8岁男孩和7岁男孩的滤泡变异型和常规型复发性PTC,并讨论了儿科患者与成人患者不同的临床病理和分子特征。
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引用次数: 3
Heterotopic pancreas in omphalomesenteric duct remnant results in persistent umbilical discharge. 脐肠系管残余的异位胰腺导致持续的脐带放电。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.323
Eunhyang Park, Hyojin Kim, Kyu Whan Jung, Jin-Haeng Chung
Umbilical discharge in infancy is a common pediatric problem and usually attributed to infection or an umbilical granuloma. However, it is important to investigate if such discharge is due to an underlying congenital abnormality such as umbilical hernia ulceration, urachal remnant, or omphalomesenteric duct remnant, because corrective surgical intervention may then be required. Omphalomesenteric duct remnant can cause umbilical discharge generally through patency between the gut and umbilicus. However, though rare, umbilical discharge may be due to the presence of heterotopic pancreas. The prevalence of omphalomesenteric duct remnant is only 2% of the population, and most of them remain asymptomatic. The present case is an infant with persistent umbilical discharge caused by heterotopic pancreatic tissue in a remnant omphalomesenteric duct. To the best of our knowledge, this is the first such case report in Korea. A 3-month-old female infant presented with persistent umbilical discharge since birth. The infant was born through normal vaginal delivery following an uneventful gestational period and had no congenital anomalies. She had been gaining weight well and had no family history of genitourinary or gastrointestinal problems. Ultrasonography of the abdomen revealed an isoechoic tract posterior to the umbilicus, and the diagnosis of urachal remnant was suspected. On physical examination, small droplets of clear fluid constantly discharged from a normallooking umbilicus. Laboratory examination results were within normal limits. Under general anesthesia, an incision was made below umbilicus. Surgical exploration showed a fibrous sinus posterior to the umbilicus which was attached to the inner aspect of the umbilicus and the outer wall of the ileum by a fi brous band. Fibrous tissue was excised close to both ends, and the rest was ligated by suture tie. The excised specimen was a 7×6×5-mm-sized whitish fibrous tissue. Histologically, the excised specimen included pancreatic tissue with some small intestinal mucosa and fibrous extracellular components (Fig. 1). Both exocrine and endocrine pancreatic tissues were observed, including acini, ducts, and islets of Langerhans. Acini were separated into lobules by connective tissue. Intercalated ducts were lined by simple low cuboidal epithelium (Fig. 2). The patient was discharged without any postoperative complications and is currently alive without any sequelae.
{"title":"Heterotopic pancreas in omphalomesenteric duct remnant results in persistent umbilical discharge.","authors":"Eunhyang Park,&nbsp;Hyojin Kim,&nbsp;Kyu Whan Jung,&nbsp;Jin-Haeng Chung","doi":"10.4132/KoreanJPathol.2014.48.4.323","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2014.48.4.323","url":null,"abstract":"Umbilical discharge in infancy is a common pediatric problem and usually attributed to infection or an umbilical granuloma. However, it is important to investigate if such discharge is due to an underlying congenital abnormality such as umbilical hernia ulceration, urachal remnant, or omphalomesenteric duct remnant, because corrective surgical intervention may then be required. Omphalomesenteric duct remnant can cause umbilical discharge generally through patency between the gut and umbilicus. However, though rare, umbilical discharge may be due to the presence of heterotopic pancreas. The prevalence of omphalomesenteric duct remnant is only 2% of the population, and most of them remain asymptomatic. The present case is an infant with persistent umbilical discharge caused by heterotopic pancreatic tissue in a remnant omphalomesenteric duct. To the best of our knowledge, this is the first such case report in Korea. A 3-month-old female infant presented with persistent umbilical discharge since birth. The infant was born through normal vaginal delivery following an uneventful gestational period and had no congenital anomalies. She had been gaining weight well and had no family history of genitourinary or gastrointestinal problems. Ultrasonography of the abdomen revealed an isoechoic tract posterior to the umbilicus, and the diagnosis of urachal remnant was suspected. On physical examination, small droplets of clear fluid constantly discharged from a normallooking umbilicus. Laboratory examination results were within normal limits. Under general anesthesia, an incision was made below umbilicus. Surgical exploration showed a fibrous sinus posterior to the umbilicus which was attached to the inner aspect of the umbilicus and the outer wall of the ileum by a fi brous band. Fibrous tissue was excised close to both ends, and the rest was ligated by suture tie. The excised specimen was a 7×6×5-mm-sized whitish fibrous tissue. Histologically, the excised specimen included pancreatic tissue with some small intestinal mucosa and fibrous extracellular components (Fig. 1). Both exocrine and endocrine pancreatic tissues were observed, including acini, ducts, and islets of Langerhans. Acini were separated into lobules by connective tissue. Intercalated ducts were lined by simple low cuboidal epithelium (Fig. 2). The patient was discharged without any postoperative complications and is currently alive without any sequelae.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2014-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.4.323","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32662801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Usefulness of Nuclear Protein in Testis (NUT) Immunohistochemistry in the Cytodiagnosis of NUT Midline Carcinoma: A Brief Case Report. 睾丸核蛋白(NUT)免疫组织化学在NUT中线癌细胞诊断中的价值:一个简短的病例报告。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.335
Heae Surng Park, Yoon Sung Bae, Sun Och Yoon, Beom Jin Lim, Hyun Jun Hong, Jae Y Ro, Soon Won Hong
Nuclear protein in testis (NUT) midline carcinomas are uncommon, recently described, fatal neoplasm that are characterized by rearrangement of the NUT gene on 15q14.1 Since the first case of NUT midline carcinoma was reported as an undifferentiated carcinoma with a t(15;19) translocation in 1991,2 more than 50 cases have been reported.3 Because of the unique chromosomal translocation and predilection for occurrence in midline structures, they have been termed NUT midline carcinomas. However, tumors outside the midline have been reported, including the salivary gland, bladder, and other sites.1,3,4,5 We encountered a case of NUT midline carcinoma confirmed by NUT specific immunohistochemistry (IHC) using cytologic and histologic specimens. Herein, we present the first case report on immunocytologic features of NUT midline carcinoma arising in the parotid gland.
{"title":"Usefulness of Nuclear Protein in Testis (NUT) Immunohistochemistry in the Cytodiagnosis of NUT Midline Carcinoma: A Brief Case Report.","authors":"Heae Surng Park,&nbsp;Yoon Sung Bae,&nbsp;Sun Och Yoon,&nbsp;Beom Jin Lim,&nbsp;Hyun Jun Hong,&nbsp;Jae Y Ro,&nbsp;Soon Won Hong","doi":"10.4132/KoreanJPathol.2014.48.4.335","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2014.48.4.335","url":null,"abstract":"Nuclear protein in testis (NUT) midline carcinomas are uncommon, recently described, fatal neoplasm that are characterized by rearrangement of the NUT gene on 15q14.1 Since the first case of NUT midline carcinoma was reported as an undifferentiated carcinoma with a t(15;19) translocation in 1991,2 more than 50 cases have been reported.3 Because of the unique chromosomal translocation and predilection for occurrence in midline structures, they have been termed NUT midline carcinomas. However, tumors outside the midline have been reported, including the salivary gland, bladder, and other sites.1,3,4,5 We encountered a case of NUT midline carcinoma confirmed by NUT specific immunohistochemistry (IHC) using cytologic and histologic specimens. Herein, we present the first case report on immunocytologic features of NUT midline carcinoma arising in the parotid gland.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2014-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.4.335","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32662310","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
The Role of TWIST in Ovarian Epithelial Cancers. TWIST在卵巢上皮癌中的作用。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.283
Kyungbin Kim, Eun Young Park, Man Soo Yoon, Dong Soo Suh, Ki Hyung Kim, Jeong Hee Lee, Dong Hoon Shin, Jee Yeon Kim, Mee Young Sol, Kyung Un Choi

Background: Epithelial-mesenchymal transition (EMT) is associated with tumor hypoxia. EMT is regulated, in part, by the action of TWIST, which inhibits of E-cadherin expression and may interfere with the p53 tumor-suppressor pathway.

Methods: We examined the expression of TWIST, E-cadherin, hypoxia-inducible factor 1α (HIF1α), and p53 by immunohistochemistry in 123 cases of ovarian epithelial cancers (OEC) to evaluate the role of TWIST in OEC. We assessed the association between protein expression and clinicopathologic parameters.

Results: The expression of TWIST, E-cadherin, HIF1α, and p53 proteins was found in 28.5%, 51.2%, 35.0%, and 29.3% of cases, respectively. TWIST expression was associated with higher histologic grade and unfavorable survival. TWIST expression was correlated with HIF1α expression and reduced E-cadherin expression. The altered HIF1α/TWIST/E-cadherin pathway was associated with lower overall survival (OS), while the co-expression of TWIST and p53 was correlated with lower progression-free survival. In the multivariate analyses, TWIST expression was an independent prognostic factor for OS.

Conclusions: Our data imply that TWIST expression could be a useful predictor of unfavorable prognosis for OEC. TWIST may affect the p53 tumor-suppressor pathway. Moreover, hypoxia-mediated EMT, which involves the HIF1α/TWIST/E-cadherin pathway may play an important role in the progression of OEC.

背景:上皮-间质转化(EMT)与肿瘤缺氧有关。EMT部分受TWIST的调控,TWIST抑制E-cadherin的表达,并可能干扰p53肿瘤抑制通路。方法:应用免疫组化方法检测123例卵巢上皮性癌(OEC)中TWIST、E-cadherin、缺氧诱导因子1α (HIF1α)和p53的表达,探讨TWIST在OEC中的作用。我们评估了蛋白表达与临床病理参数之间的关系。结果:TWIST、E-cadherin、HIF1α和p53蛋白的表达分别占28.5%、51.2%、35.0%和29.3%。TWIST的表达与较高的组织学分级和不利的生存有关。TWIST表达与HIF1α表达和E-cadherin表达降低相关。改变的HIF1α/TWIST/E-cadherin通路与较低的总生存期(OS)相关,而TWIST和p53的共同表达与较低的无进展生存期相关。在多变量分析中,TWIST表达是OS的独立预后因素。结论:我们的数据表明TWIST表达可能是OEC不良预后的有效预测因子。TWIST可能影响p53肿瘤抑制通路。此外,涉及HIF1α/TWIST/E-cadherin通路的缺氧介导的EMT可能在OEC的进展中发挥重要作用。
{"title":"The Role of TWIST in Ovarian Epithelial Cancers.","authors":"Kyungbin Kim,&nbsp;Eun Young Park,&nbsp;Man Soo Yoon,&nbsp;Dong Soo Suh,&nbsp;Ki Hyung Kim,&nbsp;Jeong Hee Lee,&nbsp;Dong Hoon Shin,&nbsp;Jee Yeon Kim,&nbsp;Mee Young Sol,&nbsp;Kyung Un Choi","doi":"10.4132/KoreanJPathol.2014.48.4.283","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2014.48.4.283","url":null,"abstract":"<p><strong>Background: </strong>Epithelial-mesenchymal transition (EMT) is associated with tumor hypoxia. EMT is regulated, in part, by the action of TWIST, which inhibits of E-cadherin expression and may interfere with the p53 tumor-suppressor pathway.</p><p><strong>Methods: </strong>We examined the expression of TWIST, E-cadherin, hypoxia-inducible factor 1α (HIF1α), and p53 by immunohistochemistry in 123 cases of ovarian epithelial cancers (OEC) to evaluate the role of TWIST in OEC. We assessed the association between protein expression and clinicopathologic parameters.</p><p><strong>Results: </strong>The expression of TWIST, E-cadherin, HIF1α, and p53 proteins was found in 28.5%, 51.2%, 35.0%, and 29.3% of cases, respectively. TWIST expression was associated with higher histologic grade and unfavorable survival. TWIST expression was correlated with HIF1α expression and reduced E-cadherin expression. The altered HIF1α/TWIST/E-cadherin pathway was associated with lower overall survival (OS), while the co-expression of TWIST and p53 was correlated with lower progression-free survival. In the multivariate analyses, TWIST expression was an independent prognostic factor for OS.</p><p><strong>Conclusions: </strong>Our data imply that TWIST expression could be a useful predictor of unfavorable prognosis for OEC. TWIST may affect the p53 tumor-suppressor pathway. Moreover, hypoxia-mediated EMT, which involves the HIF1α/TWIST/E-cadherin pathway may play an important role in the progression of OEC.</p>","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2014-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.4.283","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32662793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
Undifferentiated embryonal sarcoma in adult liver. 成人肝脏未分化胚胎性肉瘤。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.311
Won Ju Hong, Yu Na Kang, Koo Jeong Kang
Undifferentiated embryonal sarcoma (UES) is the third most common primary malignant liver tumor in children, following hepatoblastoma and hepatocellular carcinoma. UES of the liver was first named by Stocker and Ishak in 1978,1 and the majority of patients at the time ranged from 6 to 10 years of age. A recent review of the literature showed only 70 cases of UES in adults reported worldwide in 2008.2 This rare presentation is especially true for adults aged >60 years with only 14 cases of UES reported in this population until now.3,4,5,6,7 In Korea, eight cases of UES in adults have been reported: five cases were in women and four cases were in people older than 60 years.5,6,7,8 We present a new case of adult UES of the liver arising in a 67-year-old man. Like pediatric UES, the adult tumor has an unclear pathogenesis and poor prognosis.
{"title":"Undifferentiated embryonal sarcoma in adult liver.","authors":"Won Ju Hong,&nbsp;Yu Na Kang,&nbsp;Koo Jeong Kang","doi":"10.4132/KoreanJPathol.2014.48.4.311","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2014.48.4.311","url":null,"abstract":"Undifferentiated embryonal sarcoma (UES) is the third most common primary malignant liver tumor in children, following hepatoblastoma and hepatocellular carcinoma. UES of the liver was first named by Stocker and Ishak in 1978,1 and the majority of patients at the time ranged from 6 to 10 years of age. \u0000 \u0000A recent review of the literature showed only 70 cases of UES in adults reported worldwide in 2008.2 This rare presentation is especially true for adults aged >60 years with only 14 cases of UES reported in this population until now.3,4,5,6,7 In Korea, eight cases of UES in adults have been reported: five cases were in women and four cases were in people older than 60 years.5,6,7,8 We present a new case of adult UES of the liver arising in a 67-year-old man. Like pediatric UES, the adult tumor has an unclear pathogenesis and poor prognosis.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2014-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.4.311","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32662798","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Signet-ring cell carcinoma of the distal common bile duct: report of a case. 胆总管远端印戒细胞癌1例报告。
Pub Date : 2014-08-01 Epub Date: 2014-08-26 DOI: 10.4132/KoreanJPathol.2014.48.4.315
Hyung Jun Kwon, Ghil-Suk Yoon, Yong Chul Kwon, Sang Geol Kim, Ji Yun Jeong
Signet-ring cell carcinoma (SRCC) of the extrahepatic bile duct is a histologically distinct entity classified by the World Health Organization, in which cells containing intracytoplasmic mucin displacing the nucleus predominate.1 SRCC of the gastrointestinal tract is most commonly found in the stomach, and the impact of this histology on the prognosis is controversial.2,3 Well to moderately differentiated adenocarcinoma is the most common histologic type and complete resection is the only potentially curative therapy for distal bile duct cancer.4 However SRCC of extrahepatic bile duct is extremely rare, so its clinico-pathological features and impact on the prognosis are not well known. To the best of our knowledge, only three cases of SRCC of the extrahepatic bile duct have been reported in the English literature.5,6,7 Herein, we present a case of SRCC originating from the epithelium of the distal extrahepatic bile duct.
{"title":"Signet-ring cell carcinoma of the distal common bile duct: report of a case.","authors":"Hyung Jun Kwon,&nbsp;Ghil-Suk Yoon,&nbsp;Yong Chul Kwon,&nbsp;Sang Geol Kim,&nbsp;Ji Yun Jeong","doi":"10.4132/KoreanJPathol.2014.48.4.315","DOIUrl":"https://doi.org/10.4132/KoreanJPathol.2014.48.4.315","url":null,"abstract":"Signet-ring cell carcinoma (SRCC) of the extrahepatic bile duct is a histologically distinct entity classified by the World Health Organization, in which cells containing intracytoplasmic mucin displacing the nucleus predominate.1 SRCC of the gastrointestinal tract is most commonly found in the stomach, and the impact of this histology on the prognosis is controversial.2,3 \u0000 \u0000Well to moderately differentiated adenocarcinoma is the most common histologic type and complete resection is the only potentially curative therapy for distal bile duct cancer.4 However SRCC of extrahepatic bile duct is extremely rare, so its clinico-pathological features and impact on the prognosis are not well known. To the best of our knowledge, only three cases of SRCC of the extrahepatic bile duct have been reported in the English literature.5,6,7 Herein, we present a case of SRCC originating from the epithelium of the distal extrahepatic bile duct.","PeriodicalId":49936,"journal":{"name":"Korean Journal of Pathology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2014-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4132/KoreanJPathol.2014.48.4.315","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32662799","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
期刊
Korean Journal of Pathology
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