Metas-Chip precisely identifies presence of micrometastasis in live biopsy samples by label free approach

Detecting the micrometastasis is a major challenge in patients’ survival. The small volume of the biopsied tissue results in limited number of histopathological samples and might reduce the rate of accurate diagnosis even by molecular technologies. We introduce a microelectronic biochip (named Metas...

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Veröffentlicht in:Nature communications 2017-12, Vol.8 (1), p.2175-14, Article 2175
Hauptverfasser: Nikshoar, Mohammad Saeid, Khayamian, Mohammad Ali, Ansaryan, Saeid, Sanati, Hassan, Gharooni, Milad, Farahmand, Leila, Rezakhanloo, Farshad, Majidzadeh-A, Keivan, Hoseinpour, Parisa, Dadgari, Shahrzad, Kiani-M, Leila, Saqafi, Mohammad, Gity, Masoumeh, Abdolahad, Mohammad
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Sprache:eng
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Zusammenfassung:Detecting the micrometastasis is a major challenge in patients’ survival. The small volume of the biopsied tissue results in limited number of histopathological samples and might reduce the rate of accurate diagnosis even by molecular technologies. We introduce a microelectronic biochip (named Metas-Chip) to detect the micrometastasis in unprocessed liquid or solid samples. It works based on the tendency of malignant cells to track single human umbilical vein endothelial cell (HUVEC)-sensing traps. Such cells detach themselves from the biopsied sample and invade the sensing traps by inducing membrane retraction and blebbing, which result in sharp changes in electrical response of the sensing elements. Metas-Chip identified the metastasis in more than 70 breast cancer patients, in less than 5 h. Moreover it detected the metastasis in lymph nodes of nine patients whom were missed by conventional pathological procedure. Multilevel IHC and real-time polymerase chain reaction (RT-PCR) tests confirmed the diagnosis. Detecting metastatic cells in tumor/lymph node samples of breast cancer patients is extremely important for diagnosis. Here the authors develop a microelectronic biochip that detect the presence of invasive/metastatic cells in unprocessed biopsies and performs better than the current gold standards.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-017-02184-x