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. 2022 Feb 13;13(2):2552–2565. doi: 10.1080/21655979.2021.2018538

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© 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 2. — LINC00525 promoted the proliferation of colorectal cancer cells in vitro and in vivo.

(A) Cell viability was detected in SW620, SW1116 and LoVo colorectal cancer cell knocking down LINC00525. Data shown are mean ±SD (n = 3). ** P < 0.01 and *** P < 0.001 vs si-NC group.(B) Representative photographs of cell clone were taken 2 weeks after culture.(C) Comparison of the number of cell clones in SW620, SW1116 and LoVo colorectal cancer cell knocking down LINC00525. Data shown are mean ±SD (n = 3).*** P < 0.001 vs si-NC group.(D) Comparison of the weights of xenografts harvested 3 weeks after injection (n = 7). Data shown are mean ±SD (n = 3). *** P < 0.001 vs si-NC group.