Literature DB >> 36197978

POU2AF2/C11orf53 functions as a coactivator of POU2F3 by maintaining chromatin accessibility and enhancer activity.

Aileen Patricia Szczepanski1,2, Natsumi Tsuboyama1,2, Jun Watanabe3,4, Rintaro Hashizume1,3,4,5, Zibo Zhao1,2, Lu Wang1,2,5.   

Abstract

Small cell lung cancer (SCLC), accounting for around 13% of all lung cancers, often results in rapid tumor growth, early metastasis, and acquired therapeutic resistance. The POU class 2 homeobox 3 (POU2F3) is a master regulator of tuft cell identity and defines the SCLC-P subtype that lacks the neuroendocrine markers. Here, we have identified a previously uncharacterized protein, C11orf53, which is coexpressed with POU2F3 in both SCLC cell lines and patient samples. Mechanistically, C11orf53 directly interacts with POU2F3 and is recruited to chromatin by POU2F3. Depletion of C11orf53 reduced enhancer H3K27ac levels and chromatin accessibility, resulting in a reduction of POU2F3-dependent gene expression. On the basis of the molecular function of C11orf53, we renamed it as "POU Class 2 Homeobox Associating Factor 2" (POU2AF2). In summary, our study has identified a new coactivator of POU2F3 and sheds light on the therapeutic potential of targeting POU2AF2/POU2F3 heterodimer in human SCLC.

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Year:  2022        PMID: 36197978     DOI: 10.1126/sciadv.abq2403

Source DB:  PubMed          Journal:  Sci Adv        ISSN: 2375-2548            Impact factor:   14.957


  1 in total

1.  Selective regulation of tuft cell-like small cell lung cancer by novel transcriptional co-activators C11orf53 and COLCA2.

Authors:  Hui Huang; Yunyi Wang; Chen Zhou; Erdem Sendinc; Yang Shi
Journal:  Cell Discov       Date:  2022-10-18       Impact factor: 38.079

  1 in total

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