Journal Article

Alternative transcription initiation leads to expression of a novel ALK isoform in cancer

Hu, Wenhuo, Chi, Ping, Busam, Klaus J., Cao, Zhen, Zhang, Qi Fan, Postow, Michael A., Ariyan, Charlotte E., Obenauf, Anna C., Sboner, Andrea, Gao, Dong, Borsu, Laetitia, Ran, Leili, Hollmann, Travis J., Shah, Ronak H., Shukla, Shipra, Ladanyi, Marc, Fagin, James A., Zheng, Deyou, Lee, William, Wiesner, Thomas, Wong, Elissa W. P., Chen, Yu, Murali, Rajmohan, Murphy, Devan A., Merghoub, Taha, Lailler, Nathalie, Button, Julia, Wang, Lu, Scott, Sasinya N., Schwartz, Gary K., Berger, Michael F., Landa, Iñigo

2015

Overview

A novel ALK transcript expressed in a subset of human cancers, arising from a de novo alternative transcription initiation site within the ALK gene, is described; the ALK transcript encodes three protein isoforms that stimulate tumorigenesis in vivo in mouse models; resultant tumours are sensitive to treatments with ALK inhibitors, indicating a possible therapeutic avenue for patients expressing these isoforms. A novel oncogene activation mechanism Oncogenes are usually activated by genetic abberations. Ping Chi and colleagues have identified a novel isoform of the anaplastic lymphoma kinase (ALK) in a subset of human cancers, arising independently of genomic aberrations at the ALK locus through alternative transcription initiation in ALK intron 19. Tumours driven by the transcript, termed ALK ATI , are sensitive to ALK inhibitors, suggesting ALK inhibitors as possible therapeutics in patients expressing these isoforms. Activation of oncogenes by mechanisms other than genetic aberrations such as mutations, translocations, or amplifications is largely undefined. Here we report a novel isoform of the anaplastic lymphoma kinase (ALK) that is expressed in ∼11% of melanomas and sporadically in other human cancer types, but not in normal tissues. The novel ALK transcript initiates from a de novo alternative transcription initiation (ATI) site in ALK intron 19, and was termed ALK ATI . In ALK ATI -expressing tumours, the ATI site is enriched for H3K4me3 and RNA polymerase II, chromatin marks characteristic of active transcription initiation sites 1 . ALK ATI is expressed from both ALK alleles, and no recurrent genetic aberrations are found at the ALK locus, indicating that the transcriptional activation is independent of genetic aberrations at the ALK locus. The ALK ATI transcript encodes three proteins with molecular weights of 61.1, 60.8 and 58.7 kilodaltons, consisting primarily of the intracellular tyrosine kinase domain. ALK ATI stimulates multiple oncogenic signalling pathways, drives growth-factor-independent cell proliferation in vitro, and promotes tumorigenesis in vivo in mouse models. ALK inhibitors can suppress the kinase activity of ALK ATI , suggesting that patients with ALK ATI -expressing tumours may benefit from ALK inhibitors. Our findings suggest a novel mechanism of oncogene activation in cancer through de novo alternative transcription initiation.

• Publisher: Nature Publishing Group UK,Nature Publishing Group
• Subject: 13 / 13/106 / 631/67 / 631/67/1813/1634 / 631/67/395 / Alleles / Anaplastic Lymphoma Kinase / Animals / Binding sites / Cancer / Cancer therapies / Cell Line, Tumor / Cell Proliferation / Cell Transformation, Neoplastic / Development and progression / Female / Gene Expression Regulation, Neoplastic - genetics / Genes / Genetic aspects / Genetic transcription / Health aspects / HEK293 Cells / Histones - chemistry / Histones - metabolism / Humanities and Social Sciences / Humans / Introns - genetics / Isoenzymes - antagonists & inhibitors / Isoenzymes - biosynthesis / Isoenzymes - chemistry / Isoenzymes - genetics / Kinases / letter / Lymphoma / Lysine - metabolism / Melanoma / Metastasis / Methylation / Mice / Molecular Sequence Data / Molecular Weight / multidisciplinary / Neoplasms - drug therapy / Neoplasms - enzymology / Neoplasms - genetics / NIH 3T3 Cells / Oncogenes / Oncogenes - genetics / Phosphorylation / Protein Structure, Tertiary - genetics / Proteins / Receptor Protein-Tyrosine Kinases - antagonists & inhibitors / Receptor Protein-Tyrosine Kinases - biosynthesis / Receptor Protein-Tyrosine Kinases - chemistry / Receptor Protein-Tyrosine Kinases - genetics / RNA Polymerase II - metabolism / RNA, Messenger - analysis / RNA, Messenger - genetics / Science / Signal Transduction / Thyroid cancer / Transcription Initiation, Genetic / Tumorigenesis / Tumors