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Nonlinear Optical Staging of Epithelial Neoplasms

上皮肿瘤的非线性光学分期

基本信息

批准号：
8410630
负责人：
Gracie Vargas
金额：
$ 25.24万
依托单位：
UNIVERSITY OF TEXAS MED BR GALVESTON
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-04-01 至 2014-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8410630
关键词：
Address Animal Model Area Biochemical Biological Markers Biomedical Engineering Biopsy Characteristics Clinical Collagen Complex Contrast Media Detection Development Diagnostic Procedure Early Diagnosis Epithelial Epithelial Neoplasms Epithelium Evaluation Excision Extracellular Matrix Fluorescence Fluorescence Spectroscopy Fluorescent Dyes Future Generations Goals Histology Human Image Imaging Techniques Knowledge Laboratories Lesion Lesion by Stage Light Malignant Neoplasms Maps Medical Methodology Methods Microscopy Modeling Molecular Morbidity - disease rate Mouth Neoplasms Multiphoton Fluorescence Microscopy Neoplasms Neoplastic Cell Transformation Operative Surgical Procedures Optical Methods Optics Patients Premalignant Process Recording of previous events Recurrence Research Risk Signal Transduction Site Specificity Staging Stratified Squamous Epithelium Structural Protein Survival Rate Techniques Testing Texas Tissues Translations Universities Work base carcinogenesis improved in vivo malignant mouth neoplasm mortality mouth squamous cell carcinoma multidisciplinary neoplastic novel optical imaging second harmonic spatiotemporal spectroscopic imaging tumor progression

项目摘要

DESCRIPTION (provided by applicant): The long-term goal of the proposed research is to develop a novel multimodal approach for optical staging of epithelial precancerous lesions and early neoplasms using the nonlinear optical imaging techniques of multiphoton microscopy (MPM) and second harmonic generation microscopy (SHGM). The research will combine the ability to detect and map endogenous tissue autofluorescence in the epithelium and stroma assessed by MPM with second harmonic generation originating specifically from stromal structural proteins, primarily collagen. Significant optical and microstructural alterations have been documented with neoplastic transformation. However, while a number of previous optical methods have been associated with high sensitivity to neoplastic change, they generally lacked specificity in detection and staging. It is anticipated that the ability to assess both microarchitectural and optical changes in-depth by MPM-SHGM, resulting in image representations on a level similar to histology, will result in higher specificity than previous techniques. The MPM-SHGM technique will be developed and refined in a model of oral squamous cell carcinoma (which occurs in a site suited for the development of optical assessment techniques) and will be applicable to other epithelial neoplasms at various tissue sites in the future. In brief, the project will involve the a) the spatiotemporal study of epithelial neoplastic transformation in vivo in order to better understand alterations in endogenous optical signals revealed by MPM-SHGM and to identify significant image-based parameters which may serve as markers of neoplastic progression, b) the development and refinement of a noninvasive staging methodology by MPM-SHGM which may assist in guiding surgical resection and in surveillance of patients at risk for recurrence, and c) evaluation of the combination of exogenous contrast agents with MPM-SHGM to reveal molecular-specific signal alterations indicative of neoplastic potential. This research addresses a significant problem in staging of epithelial neoplasms. There is a need for highly specific noninvasive detection methods to assist in the early staging of epithelial neoplasms in general because the chances of patient survival are directly correlated to the stage at which epithelial cancers are detected and treated. Oral cancer, the 6th most common cancer in the world and one which is associated with a five-year survival rate of only 50-55%, is associated with a significant local recurrence rate for which early detection and staging is of primary importance to patient survival. Despite occurring in a highly accessible tissue for inspection high mortality and morbidity rates, particularly following recurrence, indicate the need for improved detection and staging of oral neoplasia.

描述(申请人提供)：拟议研究的长期目标是开发一种新的多模式方法，用于使用多光子显微镜(MPM)和二次谐波产生显微镜(SHGM)的非线性光学成像技术对上皮癌前病变和早期肿瘤进行光学分期。这项研究将结合MPM评估的检测和定位上皮和间质中内源性组织自发荧光的能力，以及来自间质结构蛋白(主要是胶原蛋白)的二次谐波产生。随着肿瘤的转化，已经记录了显著的光学和显微结构变化。然而，虽然以前的一些光学方法与肿瘤变化的高度敏感性有关，但它们在检测和分期方面通常缺乏特异性。预计通过MPM-SHGM深入评估微结构和光学变化的能力，导致图像表示在类似于组织学的水平上，将导致比以前的技术更高的特异性。MPM-SHGM技术将在口腔鳞状细胞癌(发生在适合发展光学评估技术的部位)的模型中进行开发和改进，并将在未来适用于不同组织部位的其他上皮性肿瘤。简而言之，该项目将涉及a)体内上皮肿瘤转化的时空研究，以更好地了解MPM-SHGM揭示的内源性光学信号的变化，并确定可作为肿瘤进展标志的重要的基于图像的参数，b)开发和改进MPM-SHGM的非侵入性分期方法，其可能有助于指导手术切除和监测复发风险的患者，以及c)评估外源性造影剂与MPM-SHGM的组合，以揭示指示肿瘤潜力的分子特异性信号变化。这项研究解决了上皮性肿瘤分期的一个重要问题。一般情况下，需要高度特异的非侵入性检测方法来辅助上皮性肿瘤的早期分期，因为患者的生存机会与检测和治疗上皮性癌症的阶段直接相关。口腔癌是世界上第六大常见癌症，其五年生存率仅为50%-55%。口腔癌与显著的局部复发率有关，早期发现和分期对患者生存至关重要。尽管发生在便于检查的组织中，但死亡率和发病率很高，特别是在复发之后，这表明需要改进口腔肿瘤的检测和分期。

项目成果

期刊论文数量（10）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Label-Free Imaging and Histo-Optical Evaluation of Head and Neck Cancers with Multiphoton Autofluorescence Microscopy.

具有多光自动荧光显微镜的头颈癌的无标签成像和组织光学评估。

DOI：
10.3390/cancers15041302
发表时间：
2023-02-18
期刊：
Cancers
影响因子：
5.2
作者：
通讯作者：

In-vivo nonlinear optical microscopy (NLOM) of epithelial-connective tissue interface (ECTI) reveals quantitative measures of neoplasia in hamster oral mucosa.

体内非线性光学显微镜（NLOM）的上皮组织界面（ECTI）揭示了仓鼠口腔粘膜中肿瘤的定量测量。

DOI：
10.1371/journal.pone.0116754
发表时间：
2015
期刊：
PloS one
影响因子：
3.7
作者：
Pal R;Yang J;Ortiz D;Qiu S;Resto V;McCammon S;Vargas G
通讯作者：
Vargas G

Remodeling of the Epithelial-Connective Tissue Interface in Oral Epithelial Dysplasia as Visualized by Noninvasive 3D Imaging.

DOI：
10.1158/0008-5472.can-16-0252
发表时间：
2016-08-15
期刊：
Cancer research
影响因子：
11.2
作者：
Pal R;Shilagard T;Yang J;Villarreal P;Brown T;Qiu S;McCammon S;Resto V;Vargas G
通讯作者：
Vargas G

In vivo layer-resolved characterization of oral dysplasia via nonlinear optical micro-spectroscopy.