Page 92 - IJB-9-4
P. 92

International Journal of Bioprinting                                       Laser transfer for CTC isolation

























































            Figure 7. TP53 and BRAF mutations detected in MDA-MB-231 cells isolated by BA-LIFT technology. (A) Agarose gel of PCR reaction products from the
            amplification of exon 9 of the TP53 in a MDA-MB-231 cell (lane 1), 25 MDA-MB-231 cells (lane 2), 1000 MDA-MB-231 control (lane 3), 1000 PBMCs
            control (lane 4), and negative control (lane 5) compared to a DNA ladder (lane L). (B) Electropherogram showing the partial sequence of exon 9 of TP53
            in a MDA-MB-231 cell (B.1), 25 MDA-MB-231 cells (B.2), 1000 MDA-MB-231 cells control (B.3), and 1000 PBMCs control (B.4). The presence of thymine
            and absence of guanine at position 839 of exon 9 of TP53 gene (homozygous) can be observed in cases B.1, B.2, and B.3. The mutation is not observed in
            B.4. (C) Agarose gel of PCR reaction products from the amplification of exon 11 of BRAF gene in a MDA-MB-231 cell (lane 1), 25 MDA-MB-231 cells (lane
            2), 1000 MDA-MB-231 control (lane 3), 1000 PBMCs control (lane 4), and negative control (lane 5) compared to a DNA ladder (lane L). (D) Electrophero-
            gram showing the partial sequence of exon 11 of BRAF gene in a MDA-MB-231 cell (D.1), 25 MDA-MB-231 cells (D.2), 1000 MDA-MB-231 cells control
            (B.3), and 1000 PBMCs control (B.4). The presence of guanine and thymine at position 1391 of exon 11 of BRAF gene (heterozygous) can be observed in
            cases B.1, B.2 and B.3. The mutation is not observed in B.4.

            would help to improve the molecular characterization of   The approach followed in this work would preserve cells
            the tumor, it could be used to identify new treatment targets   for any direct irradiation of the laser light, and the negative
            and select the most appropriate therapies for each stage of   selection approach followed would maintain the CTCs free of
            the disease. Evaluation of biomarker panels from a liquid   any direct labeling, preserving the cells in perfect condition
            biopsy may enlarge the molecular landscape of primary   for further culture, characterization, or analysis (Figure 9).
            and metastatic lesions while offering the opportunity to   Therefore, this approach for CTCs isolation presents a relevant
            evaluate molecular evolution of a tumor as a real-time film.  tool to deepen the study of single CTCs at molecular level.


            Volume 9 Issue 4 (2023)                         84                         https://doi.org/10.18063/ijb.720
   87   88   89   90   91   92   93   94   95   96   97