Multilevel genomics of colorectal cancers with microsatellite instability-clinical impact of JAK1 mutations and consensus molecular subtype 1

• Published in: Genome medicine 2017-05, Vol.9 (1), p.46-46, Article 46
• Main Authors: Sveen, Anita, Johannessen, Bjarne, Tengs, Torstein, Danielsen, Stine A, Eilertsen, Ina A, Lind, Guro E, Berg, Kaja C G, Leithe, Edward, Meza-Zepeda, Leonardo A, Domingo, Enric, Myklebost, Ola, Kerr, David, Tomlinson, Ian, Nesbakken, Arild, Skotheim, Rolf I, Lothe, Ragnhild A
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - genetics; Colorectal Neoplasms - metabolism; Computer applications; Consensus molecular subtypes; Cytotoxicity; Deoxyribonucleic acid; Development and progression; DNA; DNA Mutational Analysis; DNA repair; Endometrial cancer; Female; Gastrointestinal diseases; Gene expression; Gene Expression Profiling; Gene mutation; Gene regulation; Genetic aspects; Genomes; Genomic analysis; Genomics; Humans; Immunogenicity; Immunotherapy resistance; JAK1; Janus kinase; Janus Kinase 1 - genetics; Kinases; Male; Medical prognosis; Metastases; Metastasis; Microsatellite Instability; Middle Aged; Mismatch repair; Mutation; Neoantigens; Patients; PD-1 protein; Transcription; Tumors
• ISSN: 1756-994X; 1756-994X
• DOI: 10.1186/s13073-017-0434-0

Approximately 15% of primary colorectal cancers have DNA mismatch repair deficiency, causing a complex genome with thousands of small mutations-the microsatellite instability (MSI) phenotype. We investigated molecular heterogeneity and tumor immunogenicity in relation to clinical endpoints within this distinct subtype of colorectal cancers. A total of 333 primary MSI+ colorectal tumors from multiple cohorts were analyzed by multilevel genomics and computational modeling-including mutation profiling, clonality modeling, and neoantigen prediction in a subset of the tumors, as well as gene expression profiling for consensus molecular subtypes (CMS) and immune cell infiltration. Novel, frequent frameshift mutations in four cancer-critical genes were identified by deep exome sequencing, including in CRTC1, BCL9, JAK1, and PTCH1. JAK1 loss-of-function mutations were validated with an overall frequency of 20% in Norwegian and British patients, and mutated tumors had up-regulation of transcriptional signatures associated with resistance to anti-PD-1 treatment. Clonality analyses revealed a high level of intra-tumor heterogeneity; however, this was not associated with disease progression. Among the MSI+ tumors, the total mutation load correlated with the number of predicted neoantigens (P = 4 × 10 ), but not with immune cell infiltration-this was dependent on the CMS class; MSI+ tumors in CMS1 were highly immunogenic compared to MSI+ tumors in CMS2-4. Both JAK1 mutations and CMS1 were favorable prognostic factors (hazard ratios 0.2 [0.05-0.9] and 0.4 [0.2-0.9], respectively, P = 0.03 and 0.02). Multilevel genomic analyses of MSI+ colorectal cancer revealed molecular heterogeneity with clinical relevance, including tumor immunogenicity and a favorable patient outcome associated with JAK1 mutations and the transcriptomic subgroup CMS1, emphasizing the potential for prognostic stratification of this clinically important subtype. See related research highlight by Samstein and Chan 10.1186/s13073-017-0438-9.