Journal of Innovative Optical Health Sciences, 2014, 7 (1): 1350056, Published Online: Jan. 10, 2019  

DISTINGUISHING BETWEEN HYPERPLASTIC AND ADENOMATOUS POLYPS AND NORMAL COLONIC MUCOSA BY USING MULTIPHOTON LASER SCANNING MICROSCOPY

Author Affiliations
1 Institute of Laser and Optoelectronics Technology Fujian Provincial Key Laboratory for Photonics Technology Key Laboratory of Optoelectronic Science and Technology for Medicine of Ministry of Education Fujian Normal University, Fuzhou 350007, P. R. China
2 Department of Pathology The Affiliated Union Hospital Fujian Medical University, Fuzhou 350001, P. R. China
3 Department of Colorectal Surgery The Affiliated Union Hospital Fujian Medical University, Fuzhou 350001, P. R. China
Abstract
Precisely distinguishing between hyperplastic and adenomatous polyps and normal human colonic mucosa at the cellular level is of great medical significance. In this work, multiphoton laser scanning microscopy (MPLSM) was used to obtain the high-contrast images and the morphological characteristics from normal colonic mucosa, hyperplastic polyps and tubular adenoma. By integrating the length and area measurement tools and computing tool, we quantified the difference of crypt morphology and the alteration of nuclei in normal and diseased human colonic mucosa. Our results demonstrated that the morphology of crypts had an obvious tendency to cystic dilatation or elongated in hyperplastic polyps and tubular adenoma. The content and number of mucin droplets of the scattered goblet cells had a piecemeal reduction in hyperplastic polyps and a large decrease in tubular adenoma. The nuclei of epithelial cells might be elongated and pseudostratified, but overt dysplasia was absent in hyperplastic polyps. Nevertheless, the nuclei showed enlarged, crowded, stratified and a rod-like structure, with loss of polarity in tubular adenoma. These results suggest that MPLSM has the capacity to distinguish between hyperplastic and adenomatous polyps and normal human colonic mucosa at the cellular level.
References

[1] M. M. Center, A. Jemal, R. A. Smith, E. Ward, "Worldwide variations in colorectal cancer," CA Cancer J. Clin. 59, 366–378 (2009).

[2] L. J. Burge, "Colorectal polyps and other precursor lesions: Need for an expanded view," Gastroenterol. Clin. North Am. 3, 959–970 (2002).

[3] B. C. Morson, "Precancerous lesions of the colon and rectum: Classification and controversial issues," J. Am. Med. Assoc. 179, 316–321 (1962).

[4] D. E. Aust, G. B. Baretton, "Serrated polyps of the colon and rectum (hyperplastic polyps, sessile serrated adenomas, traditional serrated adenomas, and mixed polyps) — proposal for diagnostic criteria," Virchows Arch. 457, 291–297 (2010).

[5] D. Moussata, "The confocal laser endomicroscopy," Acta Endosc. 39, 448–451 (2009).

[6] A. Hoffman, M. Goetz, M. Vieth, P. R. Galle, M. F. Neurath, R. Kiesslich "Confocal laser endomicroscopy: Technical status and current indications," Endoscopy 38, 1275–1283 (2006).

[7] G. D. D. Palma, "Confocal laser endomicroscopy in the "in vivo" histological diagnosis of the gastrointestinal tract," World J. Gastroenterol. 15, 5770– 5775 (2009).

[8] A. M. Buchner, M. W. Shahid, M. G. Heckman, M. Krishna, M. Ghabril, M. Hasan, J. E. Crook, V. Gomez, M. Raimondo, T. Woodward, H. C. Wolfsen, M. B. Wallace, "Comparison of probebased confocal laser endomicroscopy with virtual chromoendoscopy for classification of colon polyps," Gastroenterology 138, 834–842 (2010).

[9] W. R. Zipfel, R. M. Williams, R. Christie, A. Y. Nikitin, B. T. Hyman, W. W. Webb, "Live tissue intrinsic emission microscopy using multiphotonexcited native fluorescence and second harmonic generation," Proc. Natl. Acad. Sci. USA 100, 7075– 7080 (2003).

[10] M. C. Skala, K. M. Riching, A. Gendron-Fitzpatrick, J. Eickhoff, K. W. Eliceiri, J. G. White, N. Ramanujam, "In vivo multiphoton microscopy of NADH and FAD redox states, fluorescence lifetimes, and cellular morphology in precancerous epithelia," Proc. Natl. Acad. Sci. USA 104, 19494–19499 (2007).

[11] P. T. C. So, C. Y. Dong, B. R. Masters, K. M. Berland, "Two-photon excitation fluorescence microscopy," Annu. Rev. Biomed. Eng. 2, 399–429 (2000).

[12] S. M. Zhuo, L. Q. Zheng, J. X. Chen, S. S. Xie, X. Q. Zhu, X. S. Jiang, "Depth-cumulated epithelial redox ratio and stromal collagen quantity as quantitative intrinsic indicators for differentiating normal, in- flammatory, and dysplastic epithelial tissues," Appl. Phys. Lett. 97, 173701–173704 (2010).

[13] P. J. Campagnola, L. M. Loew, "Second-harmonic imaging microscopy for visualizing biomolecular arrays in cells, tissues and organisms," Nat. Biotechnol. 21, 1356–1360 (2003).

[14] V. A. Hovhannisyan, P. J. Su, S. J. Lin, C. Y. Dong, "Quantifying thermodynamics of collagen thermal denaturation by second harmonic generation imaging," Appl. Phys. Lett. 94, 233902–233905 (2009).

[15] R. Cicchi, A. Crisci, A. Cosci, G. Nesi, D. Kapsokalyvas, S. Giancane, M. Carini, F. S. Pavone, "Time- and spectral-resolved two-photon imaging of healthy bladder mucosa and carcinoma in situ," Opt. Express 18, 3840–3849 (2010).

[16] S. M. Zhuo, J. M. Chen, T. S. Luo, D. S. Zou, J. J. Zhao, "Multimode nonlinear optical imaging of the dermis in ex vivo human skin based on the combination of multichannel mode and Lambda mode," Opt. Express 14, 7810–7820 (2006).

[17] J. X. Chen, S. M. Zhuo, R. Chen, X. S. Jiang, S. S. Xie, Q. L. Zou, "Depth-resolved spectral imaging of rabbit oesophageal tissue based on two-photon excited fluorescence and second-harmonic generation," New J. Phys. 9, 212 (2007).

[18] M. Koike, K. Inada, H. Nakanishi, A. Matsuura, S.Nakamura,M. Tatematsu, "Cellular differentiation status of epithelial polyps of the colorectum: The gastric foveolar cell-type in hyperplastic polyps," Histopathology 42, 357–364 (2003).

[19] S. J. Winawer, M. J. O'Brien, J. D. Waye, O. Kronborg, J. Bond, P. Frühmorgen, L. H. Sobin, R. Burt, A. Zauber, B. Morson, "Risk and surveillance of individuals with colorectal polyps. Who Collaborating Centre for the prevention of colorectal cancer," Bull. World Health Organ 68, 789–795 (1990).

[20] K. Wallace, J. A. Baron, M. R. Karagas, B. F. Cole, T. Byers, M. A. Beach, L. H. Pearson, C. A. Burke, W. B. Silverman, R. Sandler, "The association of physical activity and body mass index with the risk of large bowel polyps," Cancer Epidemiol. Biomarkers Prev. 14, 2082–2086 (2005).

[21] K. Melican, A. Richter-Dahlfors, "Real-time live imaging to study bacterial infections it in vivo," Curr. Opin. Microbiol. 12, 31–36 (2009).

[22] B. A. Flusberg, E. D. Cocker, W. Piyawattanametha, J. C. Jung, E. L. M. Cheung, M. J. Schnitzer, "Fiber-optic fluorescence imaging," Nat. Methods 2, 941–950 (2005).

HONGSHENG LI, CHANGYIN FENG, ZHIFEN CHEN, YINGHONG YANG, WEIZHONG JIANG, SHUANGMU ZHUO, XIAOQIN ZHU, GUOXIAN GUAN, JIANXIN CHEN. DISTINGUISHING BETWEEN HYPERPLASTIC AND ADENOMATOUS POLYPS AND NORMAL COLONIC MUCOSA BY USING MULTIPHOTON LASER SCANNING MICROSCOPY[J]. Journal of Innovative Optical Health Sciences, 2014, 7(1): 1350056.

关于本站 Cookie 的使用提示

中国光学期刊网使用基于 cookie 的技术来更好地为您提供各项服务,点击此处了解我们的隐私策略。 如您需继续使用本网站,请您授权我们使用本地 cookie 来保存部分信息。
全站搜索
您最值得信赖的光电行业旗舰网络服务平台!