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. 2021 Jun 24;11:695770. doi: 10.3389/fonc.2021.695770

Figure 1.

Figure 1

Homozygous Deletions in the p21.3 region of chromosome 9 in MPM and NSCLC. (A) Schematic representation of genes present in the p21.3 region of chromosome 9 between positions 21,000,000 and 22,200,000 drawn from UCSC Genome Browser (https://genome.ucsc.edu/). (B) Oncoprint representation of CDKN2A, CDKN2B, MTAP, IFNA2 and IFNB1 genomic alterations found in tumor samples of 82 MPM patients. Oncoprint was performed with cbioportals website (http://www.cbioportal.org/) using TCGA Pancancer atlas data. (C) Oncoprint representation of CDKN2A, CDKN2B, MTAP, IFNA2 and IFNB1 genomic alterations found in tumor samples of 1144 NSCLC patients. Oncoprint was performed with cbioportals website (http://www.cbioportal.org/) using TCGA Pan lung cancer data. Only the patients with at least one genomic alteration in the five genes are shown. ADC, adenocarcinoma; SqCC, squamous cell carcinoma.