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. 2018 Mar 20;17:1533033818764499. doi: 10.1177/1533033818764499

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© The Author(s) 2018

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 4. — Agarose DNA electrophoresis of polymerase chain reaction (PCR) amplification products from complementary DNA (Cdna) of tumor slices resistant or sensitive to antineoplastic treatment (upper panels), arrows are indicating the expected products. Bands outer the expected size were considered PCR artifacts, and the 1 kb plus DNA ladder was used. Periferal Blood Mononuclear Cells (PBMCs) amplification products were included as positive controls and RPL32 as reference gene. Densitometric comparisons are shown in the lower panels. *Indicates significant differences between groups (P < .05).