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Review Article

In situ Analysis of Cancer Cells Based on DNA Signal Amplification and DNA Nanodevices

, , , , & ORCID Icon
Pages 8-19 | Published online: 15 Oct 2019
 

Abstract

Cancer is a global disease which has been disturbing researchers in medicine and seriously threatens patients’ health and lifetime around the world in the past several decades. Due to the characteristics of cancer cells, such as uncontrollable cell proliferation, cell invasion and metastasis to surrounding tissues, lower grade of differentiation, higher telomerase activity and others, it has been one of the most usual lethal factors, next to heart disease in incidence. Cancer mortality can be decreased by early diagnosis, and the people who with treatment at an early stage have an obvious improved survival rate. Consequently, early detection is significant for better understanding the pathogenesis of cancer and improving the prognosis of patients. In situ detection technique is a vital tool for imaging and cellular pathology research, which can provide effective information about tumor markers in the early cancer detection. In view of low expression of most tumor markers in the early stage of cancers, detection techniques based on DNA signal amplification and DNA nanodevices can provide a strong support for the diagnosis and detection of cancers. In this review, we summarize the research progress of different analytical techniques for detecting various tumor markers that have been reported in recent years. We compare different DNA amplification and nanodevices, then provide guidance and suggestions for better understanding in situ analysis of cancer cells.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This work was supported by the National Natural Science Foundation of China under Grant number 21575088 and 81703088; Natural Science Foundation of Shanghai under Grant number 19ZR1474200, and Medical Research Project of Jiangsu Provincial Health and Family Planning Commission, China under Grant number H2018113.

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