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      Novel Quantitative Analysis Using Optical Imaging (VELscope) and Spectroscopy (Raman) Techniques for Oral Cancer Detection

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          Abstract

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          Our study aims to develop a novel quantitative analysis method that can increase the oral cancer detection rate for screening oral cancer. We used two different optical techniques, a light-based detection technique (VELScope) and a vibrational spectroscopic technique (Raman spectroscopy). First, we analyzed and evaluated the performance of these two techniques individually using PCA–LDA, and PCA–QDA classifiers. The PCA–LDA of Raman spectroscopy had 82.9% accuracy, 80% sensitivity, and 85.7% specificity, while the region of interests on the autofluorescence images were differentiated with 90% accuracy, 100% sensitivity, and 80% specificity. Afterward, we combined both techniques and evaluated their performance. The combination of two optical techniques can differentiate the cancer and normal groups with 97.14% accuracy, 100% sensitivity, and 94.3% specificity. The main advantage of our study is that we can confirm our results by using two different techniques that are completely independent of each other. That is the reason that the combination of two techniques can increase the sensitivity and specificity.

          Abstract

          In this study, we developed a novel quantitative analysis method to enhance the detection capability for oral cancer screening. We combined two different optical techniques, a light-based detection technique (visually enhanced lesion scope) and a vibrational spectroscopic technique (Raman spectroscopy). Materials and methods: Thirty-five oral cancer patients who went through surgery were enrolled. Thirty-five cancer lesions and thirty-five control samples with normal oral mucosa (adjacent to the cancer lesion) were analyzed. Thirty-five autofluorescence images and 70 Raman spectra were taken from 35 cancer and 35 control group cryopreserved samples. The normalized intensity and heterogeneity of the 70 regions of interest (ROIs) were calculated along with 70 averaged Raman spectra. Linear discriminant analysis (LDA) and quadratic discriminant analysis (QDA) were used with principal component analysis (PCA) to differentiate the cancer and control groups (normal). The classifications rates were validated using two different validation methods, leave-one-out cross-validation (LOOCV) and k-fold cross-validation. Results: The cryopreserved normal and tumor tissues were differentiated using the PCA–LDA and PCA–QDA models. The PCA–LDA of Raman spectroscopy (RS) had 82.9% accuracy, 80% sensitivity, and 85.7% specificity, while ROIs on the autofluorescence images were differentiated with 90% accuracy, 100% sensitivity, and 80% specificity. The combination of two optical techniques differentiated cancer and normal group with 97.14% accuracy, 100% sensitivity, and 94.3% specificity. Conclusion: In this study, we combined the data of two different optical techniques. Furthermore, PCA–LDA and PCA–QDA quantitative analysis models were used to differentiate tumor and normal groups, creating a complementary pathway for efficient tumor diagnosis. The error rates of RS and VELcope analysis were 17.10% and 10%, respectively, which was reduced to 3% when the two optical techniques were combined.

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          Raman Spectroscopy of Biological Tissues

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            Near-infrared Raman spectroscopy for optical diagnosis of lung cancer.

            Raman spectroscopy is a vibrational spectroscopic technique that can be used to optically probe the molecular changes associated with diseased tissues. The objective of our study was to explore near-infrared (NIR) Raman spectroscopy for distinguishing tumor from normal bronchial tissue. Bronchial tissue specimens (12 normal, 10 squamous cell carcinoma (SCC) and 6 adenocarcinoma) were obtained from 10 patients with known or suspected malignancies of the lung. A rapid-acquisition dispersive-type NIR Raman spectroscopy system was used for tissue Raman studies at 785 nm excitation. High-quality Raman spectra in the 700-1,800 cm(-1) range from human bronchial tissues in vitro could be obtained within 5 sec. Raman spectra differed significantly between normal and malignant tumor tissue, with tumors showing higher percentage signals for nucleic acid, tryptophan and phenylalanine and lower percentage signals for phospholipids, proline and valine, compared to normal tissue. Raman spectral shape differences between normal and tumor tissue were also observed particularly in the spectral ranges of 1,000-1,100, 1,200-1,400 and 1,500-1,700 cm(-1), which contain signals related to protein and lipid conformations and nucleic acid's CH stretching modes. The ratio of Raman intensities at 1,445 to 1,655 cm(-1) provided good differentiation between normal and malignant bronchial tissue (p < 0.0001). The results of this exploratory study indicate that NIR Raman spectroscopy provides significant potential for the noninvasive diagnosis of lung cancers in vivo based on the optic evaluation of biomolecules. Copyright 2003 Wiley-Liss, Inc.
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              Oral Potentially Malignant Disorders: An Overview of More than 20 Entities

              Cancer of the oral cavity accounts for approximately 3% of all malignancies diagnosed annually in 270,000 patients world-wide. Oral cancer is the 12th most common cancer in women and the 6th in men. Many oral squamous cell carcinomas develop from potentially malignant disorders (PMDs). Lack of awareness about the signs and symptoms of oralPMDs in the general population and even healthcare providers is believed to be responsible for the diagnostic delay of these entities. The aim of this article is to update and improve the knowledge of healthcare providers about oral PMDs.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                13 November 2020
                November 2020
                : 12
                : 11
                : 3364
                Affiliations
                [1 ]Department of Electronic Engineering, Chang Gung University, Taoyuan 333, Taiwan; mjjeng@ 123456mail.cgu.edu.tw (M.-J.J.); mukta.shrm@ 123456gmail.com (M.S.)
                [2 ]Department of Otolaryngology-Head and Neck Surgery, Chang Gung Memorial Hospital, Linkou 244, Taiwan
                [3 ]Department of Computer Science and Information Engineering, Chang Gung University, Taoyuan 333, Taiwan; engglucky@ 123456gmail.com (L.S.); slwu@ 123456mail.cgu.edu.tw (S.-L.W.)
                [4 ]Department of Public Health, Chang Gung University, Taoyuan 333, Taiwan
                [5 ]Graduate Institute of Clinical Medical Sciences, Chang Gung University, Taoyuan 333, Taiwan
                [6 ]Green Technology Research Center, Chang Gung University, Guishan, Taoyuan 333, Taiwan
                [7 ]Department of Cardiology, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan
                [8 ]Department of Physics, University of Central Florida, Orlando, FL 32816, USA; Lee.Chow@ 123456ucf.edu
                Author notes
                Author information
                https://orcid.org/0000-0001-8362-510X
                https://orcid.org/0000-0003-3582-9938
                https://orcid.org/0000-0003-2174-2022
                https://orcid.org/0000-0001-7729-6848
                Article
                cancers-12-03364
                10.3390/cancers12113364
                7696965
                33202869
                8dbeafa4-d9d9-44ef-93f6-1fc7d120b206
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 September 2020
                : 10 November 2020
                Categories
                Article

                autofluorescence,cryopreserved tissue,oral cancer,raman spectroscopy,pca–lda and pca–qda

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