SCC

SCC
  • 文章类型: Journal Article
    背景:受皮肤鳞状细胞癌(cSCC)影响的患者亚组可以表现出局部侵袭性或转移性肿瘤。不同的分期分类系统当前用于cSCC。然而,在临床实践中尚未实现精确的患者风险分层.该研究旨在确定表征转移性cSCC的特定组织学和分子参数。
    方法:本研究包括转移性和非转移性cSCC患者(对照),并对其临床和组织学特征进行匹配。对来自原发性肿瘤的皮肤样品的几个组织学参数进行修正,并且还用市售小组测试770个不同基因进行基因表达谱分析。
    结果:总计,48名受试者被纳入研究(24例,24个对照);发现有67个基因在转移性和非转移性cSCC之间差异表达。大多数这样的基因参与免疫调节,皮肤完整性,血管生成,细胞迁移和增殖。
    结论:cSCC的组织学和分子谱的组合允许鉴定特定于转移性cSCC的特征,对更精确的患者风险分层有潜在的影响。
    BACKGROUND: A subset of patients affected by cutaneous squamous cell carcinoma (cSCC) can exhibit locally invasive or metastatic tumors. Different staging classification systems are currently in use for cSCC. However, precise patient risk stratification has yet to be reached in clinical practice. The study aims to identify specific histological and molecular parameters characterizing metastatic cSCC.
    METHODS: Patients affected by metastatic and non-metastatic cSCC (controls) were included in the present study and matched for clinical and histological characteristics. Skin samples from primary tumors were revised for several histological parameters and also underwent gene expression profiling with a commercially available panel testing 770 different genes.
    RESULTS: In total, 48 subjects were enrolled in the study (24 cases, 24 controls); 67 genes were found to be differentially expressed between metastatic and non-metastatic cSCC. Most such genes were involved in immune regulation, skin integrity, angiogenesis, cell migration and proliferation.
    CONCLUSIONS: The combination of histological and molecular profiles of cSCCs allows the identification of features specific to metastatic cSCC, with potential implications for more precise patient risk stratification.
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  • 文章类型: Journal Article
    阴茎鳞状细胞癌(SCC)是一种极为罕见的恶性肿瘤。它通常是由慢性人乳头瘤病毒(HPV)16和HPV18感染引起的。这项研究是为了研究p16的免疫组织化学过度表达,p16是HPV的替代标记,并评估其作为潜在诊断生物标志物的有效性。
    在这项横断面前瞻性和回顾性队列研究中,在Kasturba医学院评估了56例阴茎鳞状细胞癌(SCC)标本和5例阴茎癌前病变标本,芒格洛尔,印度,从2013年1月至2018年12月的临床和组织病理学特征来看。评估病例和对照中p16的免疫组织化学表达。临床特征之间p16表达的统计比较,组织学亚型,grade,完成了肿瘤的分期。
    p16染色模式的分析显示,在32.8%的病例中,弥漫性和强烈的细胞核和细胞质表达。在阴茎癌的HPV和非HPV亚型中,p16的表达模式存在高度显着相关性(P<0.001)。p16表达与其他预后参数如病变部位无显著相关,淋巴管浸润,神经周浸润,组织学分级,病理阶段。
    p16的表达将是区分阴茎SCC的HPV相关和非HPV相关亚型的有用工具,其可能有助于预测相应组织学亚型的侵袭性和侵袭潜力。
    UNASSIGNED: Penile squamous cell carcinoma (SCC) is an extremely rare malignancy. It is usually caused by chronic human papillomavirus (HPV) 16 and HPV 18 infections. This study was conducted to investigate the immunohistochemical overexpression of p16, a surrogate marker for HPV, and to evaluate its usefulness as a potential diagnostic biomarker.
    UNASSIGNED: In this cross-sectional prospective and retrospective cohort study, 56 penile squamous cell carcinoma (SCC) specimens and five penile premalignant specimens were evaluated in Kasturba Medical College, Mangalore, India, from January 2013- December 2018 in terms of clinical and histopathological features. Immunohistochemical expression for p16 in cases and controls was evaluated. Statistical comparison of p16 expression among clinical features, histological subtype, grade, and stages of tumor were done.
    UNASSIGNED: Analysis of the pattern of p16 staining showed diffuse and strong nuclear and cytoplasmic expression in 32.8% of the cases. There was a highly significant association (P<0.001) of pattern of p16 expression among the HPV and non-HPV subtypes of penile carcinoma. p16 expression was not significantly associated with other prognostic parameters like site of the lesion, lymphovascular invasion, perineural invasion, histologic grade, and pathologic stage.
    UNASSIGNED: Expression of p16 would be a useful tool in differentiation between the HPV-associated and non-HPV-associated subtypes of penile SCC that may be helpful in prediction of aggressiveness and invasive potential of the respective histologic subtypes.
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  • 文章类型: Letter
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  • 文章类型: Journal Article
    报告临床表现,眼前节光学相干断层扫描特征,治疗,与翼状胬肉相关的眼表鳞状细胞瘤(OSSN)的结果。
    在28个月的研究期间,对14例病例进行回顾性介入治疗。
    OSSN与翼状胬肉(n=14)共存于<1%的翼状胬肉(n=7384)。OSSN伴翼状胬肉的平均年龄为49岁(中位数,49年;范围,36至71岁)。转诊诊断包括翼状胬肉无OSSN(n=7,50%),肉芽肿(n=1,7%),光化性角化病(n=1,7%),和结膜炎(n=1,7%)。所有OSSN都是单边的,6例患者(43%)有双侧翼状胬肉。肿瘤起源于鼻部(n=8,57%),或时间(n=6,43%)象限。平均肿瘤直径为4毫米(中位数,4mm;范围,2至6毫米),平均厚度为2mm(中位数,1mm;范围,1至3毫米)。在所有(100%)病例中,都可以在眼前段光学相干断层扫描(AS-OCT)上确定OSSN和翼状胬肉之间的轮廓。所有患者接受1%外用5-氟尿嘧啶(5-FU),13例(93%)患者的肿瘤完全消退,平均2个周期(中位数,两个循环;范围,1至4个周期)。无明显不良反应。在平均11个月的随访期内,没有发现肿瘤复发(中位数为12个月;范围,1至4个月)。
    AS-OCT可以准确检测和标测伴有翼状胬肉的OSSN中的肿瘤范围,和局部5-FU产生优异的肿瘤控制。
    UNASSIGNED: To report the clinical presentation, anterior segment optical coherence tomography features, treatment, and outcomes of ocular surface squamous neoplasia (OSSN) associated with pterygium.
    UNASSIGNED: Retrospective interventional series of 14 cases in a 28-month study period.
    UNASSIGNED: OSSN was coexistent with pterygium (n = 14) in < 1% of all pterygia (n = 7384). The mean age at the presentation of OSSN with pterygium was 49 years (median, 49 years; range, 36 to 71 years). Referral diagnosis included pterygium sans OSSN (n = 7, 50%), granuloma (n = 1, 7%), actinic keratosis (n = 1, 7%), and conjunctivitis (n = 1, 7%). All OSSNs were unilateral, and six patients (43%) had bilateral pterygia. Tumors arose from the nasal (n = 8, 57%), or temporal (n = 6, 43%) quadrants. The mean tumor diameter was 4 mm (median, 4 mm; range, 2 to 6 mm), and the mean thickness was 2 mm (median, 1 mm; range, 1 to 3 mm). The delineation between OSSN and pterygium could be identified on anterior segment optical coherence tomography (AS-OCT) in all (100%) cases. All patients received 1% topical 5-fluorouracil (5-FU), and complete tumor regression was achieved in 13 (93%) cases with a mean number of 2 cycles (median, two cycles; range, 1 to 4 cycles). There were no significant adverse effects. No tumor recurrence was noted over a mean follow-up period of 11 months (median 12 months; range, 1 to 4 months).
    UNASSIGNED: AS-OCT allows accurate detection and mapping of tumor extent in OSSN with coexistent pterygium, and topical 5-FU yields excellent tumor control.
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  • 文章类型: Journal Article
    非小细胞肺癌(NSCLC)由于其异质性而面临挑战,需要精确的组织病理学分型和预后以做出最佳治疗决策。分子标记作为一种潜在的解决方案出现,克服了传统方法的局限性,并支持诊断-治疗干预措施。在这项研究中,我们验证了六个基因(MIR205HG,KRT5,KRT6A,KRT6C,SERPINB5和DSG3),先前在我们团队开发的53个基因签名中鉴定,利用基因表达微阵列技术。对140个充分表征的早期NSCLC样本的实时PCR显示,与腺癌(ADC)相比,鳞状细胞癌(SCC)中所有六个基因的大幅上调。不管临床因素。逻辑回归模型的决策边界证明了大多数基因的SCC和ADC之间相对表达水平的有效分离。不包括KRT6C。Logistic回归和梯度提升决策树分类器,整合了所有六个经过验证的基因,在区分NSCLC亚型方面表现显著(AUC分别为0.8930和0.8909)。然而,我们的调查显示,基因表达谱未能对早期NSCLC的进展产生预测价值.我们的分子诊断模型显示了NSCLC详尽分子表征的潜力,随后告知个性化治疗决策,并提高患者的临床管理和预后标准。
    Non-small-cell lung cancer (NSCLC) poses a challenge due to its heterogeneity, necessitating precise histopathological subtyping and prognostication for optimal treatment decision-making. Molecular markers emerge as a potential solution, overcoming the limitations of conventional methods and supporting the diagnostic-therapeutic interventions. In this study, we validated the expression of six genes (MIR205HG, KRT5, KRT6A, KRT6C, SERPINB5, and DSG3), previously identified within a 53-gene signature developed by our team, utilizing gene expression microarray technology. Real-time PCR on 140 thoroughly characterized early-stage NSCLC samples revealed substantial upregulation of all six genes in squamous cell carcinoma (SCC) compared to adenocarcinoma (ADC), regardless of clinical factors. The decision boundaries of the logistic regression model demonstrated effective separation of the relative expression levels between SCC and ADC for most genes, excluding KRT6C. Logistic regression and gradient boosting decision tree classifiers, incorporating all six validated genes, exhibited notable performance (AUC: 0.8930 and 0.8909, respectively) in distinguishing NSCLC subtypes. Nevertheless, our investigation revealed that the gene expression profiles failed to yield predictive value regarding the progression of early-stage NSCLC. Our molecular diagnostic models manifest the potential for an exhaustive molecular characterization of NSCLC, subsequently informing personalized treatment decisions and elevating the standards of clinical management and prognosis for patients.
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  • 文章类型: Journal Article
    需要开发用于山羊乳腺炎管理的工具并测量挤奶机对乳头的影响。红外热成像(IRT),如奶牛所示,是早期乳腺炎检测的良好候选者,并专注于挤奶设备和与潜在问题有关的设置。这项研究的目的是测试IRT以检测乳房炎症以及机械挤奶对乳头的影响与炎症状态有关,udder平衡,高山山羊的乳头形状。比较了三个商品群的551只山羊在挤奶前后的IRT光谱及其各自的SCC(体细胞计数)。我们发现logSCC和IRT测量或挤奶反应之间没有回归或趋势,甚至在高度发炎的山羊乳房中。挤奶效果显著(p<0.05),挤奶后全球温度降低,但是乳头部分和不平衡的半乳之间存在差异。在乳头孔处观察到皮肤温度的最高降低(-1.06±0.05),在乳头桶处最低(-0.37±0.05)。长桶的乳头表现出更多的IRT反应,这清楚地表明对所用衬垫的适应性差。总之,IRT无法检测到乳腺炎,但它是一个很好的工具来诊断挤奶机的效果,以适应挤奶设备和设置山羊和提高他们的福利。
    There is a need to develop tools for mastitis management in goats and to measure the effects of milking machines on teats. Infrared thermography (IRT), as shown in cows, was a good candidate for early mastitis detection and focusing on milking equipment and settings implicated in potential problems. The aim of this study was to test IRT to detect udder inflammation and the effects of mechanical milking on teats in relation to inflammation status, udder balance, and teat shape in Alpine goats. IRT spectra were compared before and after milking in 551 goats from three commercial herds compared to their individual SCC (somatic cell count). We found no regression or trend between logSCC and IRT measurement or response to milking, even in highly inflamed goat udders. The effect of milking was significant (p < 0.05) with global temperature reduction after milking, but differences were seen between teat parts and unbalanced half udders. The highest reduction in skin temperature was observed at the teat orifice (-1.06 ± 0.05) and the lowest at the teat barrel (-0.37 ± 0.05). The teats with long barrels showed more IRT reactions, which clearly indicates poor adaptation to the liners used. In conclusion, the IRT was not able to detect mastitis, but it is a good tool to diagnose the effects of the milking machine in order to adapt milking equipment and settings to the goats and improve their welfare.
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  • 文章类型: Journal Article
    背景:皮肤鳞状细胞癌(cSCC)及其惰性模拟物之间的组织病理学重叠可能导致cSCC的过度诊断。
    目的:对cSCC外阴鳞状病变的p53免疫组织化学评分系统进行初步研究。
    方法:使用针对外阴病例开发的评分系统进行p53免疫染色的一致性和可靠性,与TP53基因组测序相比,在28例皮肤病例的初始队列中进行了研究。在另外63例非典型鳞状病变中进一步评估了p53标记,包括作者分类为良性的20个非典型鳞状病变,22例诊断为无高危特征的cSCC,高危cSCC(cSCC-HR)21例。
    结果:p53标记和TP53测序的一致性为82.1%。确定了p53突变的四种阳性模式:基础,副鼻部/弥漫性,null,和细胞质。非典型p53阳性,良性鳞状病变(10%)明显低于低危cSCC(63.6%,p=0.0004)或cSCC-HR(90.5%,p<0.0001)。低风险cSCC与cSCC-HR的p53阳性无统计学意义(p=0.07)。
    结论:p53标记可能是一个有用的生物标志物,以支持cSCC的诊断和区分cSCC与非典型但良性的模拟物。
    BACKGROUND: Histopathologic overlap between cutaneous squamous cell carcinoma (cSCC) and its indolent mimics likely leads to the overdiagnosis of cSCC.
    OBJECTIVE: To perform a pilot study of the p53 immunohistochemical scoring system developed on vulvar squamous lesions in cSCC.
    METHODS: The consistency and reliability of p53 immunostaining using a scoring system developed on vulvar cases, as compared with TP53 genomic sequencing, was studied in an initial cohort of 28 cutaneous cases. p53 labeling was further assessed in an additional 63 cases of atypical squamous lesions, including 20 atypical squamous lesions classified by the authors as benign, 22 cases diagnosed as cSCC without high-risk features, and 21 cases of high-risk cSCC (cSCC-HR).
    RESULTS: The concordance of p53 labeling and TP53 sequencing was 82.1%. Four positive patterns of p53 mutation were identified: basal, parabasal/diffuse, null, and cytoplasmic. p53 positivity in atypical, benign squamous lesions (10%) was significantly lower than that of low-risk cSCC (63.6%, p = 0.0004) or cSCC-HR (90.5%, p < 0.0001). p53 positivity in low-risk cSCC versus cSCC-HR was not statistically significant (p = 0.07).
    CONCLUSIONS: p53 Labeling may be a helpful biomarker to support the diagnosis of cSCC and distinguish cSCC from atypical but benign mimics.
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  • 文章类型: Letter
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  • 文章类型: Journal Article
    常规自密实混凝土(SCC)的力学性能和抗冲击性能有待进一步提高。为了探究镀铜钢纤维自密实混凝土(CPSFRSCC)的动静态力学性能,测试了不同体积分数镀铜钢纤维(CPSF)的CPSFRSCC的静态力学性能和动态力学性能,并进行了数值实验,对实验结果进行了分析。结果表明,添加CPSF能有效改善自密实混凝土的力学性能,特别是拉伸机械性能。CPSFRSCC的静态拉伸强度呈现随CPSF体积分数的增加而增加的趋势,当CPSF体积分数为3%时达到最大值。随着CPSF体积分数的增加,CPSFRSCC的动态拉伸强度呈现先增大后减小的趋势,当CPSF的体积分数为2%时达到最大值。数值模拟结果表明,CPSFRSCC的失效形态与CPSF的含量密切相关;随着CPSF体积分数的增加,试样的断裂形态由完全断裂逐渐向不完全断裂演变。
    The mechanical properties and impact resistance of conventional self-compacting concrete (SCC) need to be further improved. In order to explore the dynamic and static mechanical properties of copper-plated steel-fiber-reinforced self-compacting concrete (CPSFRSCC), the static mechanical properties and dynamic mechanical properties of CPSFRSCC with a different volume fraction of copper-plated steel fiber (CPSF) are tested, and a numerical experiment is carried out to analyze the experimental results. The results show that the mechanical properties of self-compacting concrete (SCC) can be effectively improved by adding CPSF, especially for the tensile mechanical properties. The static tensile strength of CPSFRSCC shows a trend that increases with the increase in the volume fraction of CPSF and then reaches the maximum when the volume fraction of CPSF is 3%. The dynamic tensile strength of CPSFRSCC shows a trend that increases first and then decrease with the increase in the volume fraction of CPSF, and then reaches the maximum when the volume fraction of CPSF is 2%. The results of the numerical simulation show that the failure morphology of CPSFRSCC is closely related to the content of CPSF; with the increase in the volume fraction of CPSF, the fracture morphology of the specimen gradually evolves from complete fracture to incomplete fracture.
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  • 文章类型: Journal Article
    Fanconi anemia (FA) patients display an exacerbated risk of oral squamous cell carcinoma (OSCC) and oral potentially malignant lesions (OPMLs) at early ages. As patients have defects in their DNA repair mechanisms, standard-of-care treatments for OSCC such as radiotherapy and chemotherapy, give rise to severe toxicities. New methods for early diagnosis are urgently needed to allow for treatment in early disease stages and achieve better clinical outcomes. We conducted a prospective, longitudinal study wherein liquid biopsies from sixteen patients with no clinical diagnoses of OPML and/or OSCC were analyzed for the presence of mutations in cancer genes. The DNA from saliva and plasma were sequentially collected and deep-sequenced, and the clinical evaluation followed over a median time of approximately 2 years. In 9/16 FA patients, we detected mutations in cancer genes (mainly TP53) with minor allele frequencies (MAF) of down to 0.07%. Importantly, all patients that had mutations and clinical follow-up data after mutation detection (n = 6) developed oral precursor lesions or OSCC. The lead-time between mutation detection and tumor diagnosis ranged from 23 to 630 days. Strikingly, FA patients without mutations displayed a significantly lower risk of developing precursor lesions or OSCCs. Therefore, our diagnostic approach could help to stratify FA patients into risk groups, which would allow for closer surveillance for OSCCs or precursor lesions.
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