Informace o publikaci

STAT3 couples activated tyrosine kinase signaling to the oncogenic core transcriptional regulatory circuitry of anaplastic large cell lymphoma

Logo poskytovatele
Autoři

PRUTSCH Nicole HE Shuning BEREZOVSKAYA Alla DURBIN Adam D DHARIA Neekesh V MAHER Kelsey A MATTHEWS Jamie D HARE Lucy TURNER Suzanne Dawn STEGMAIER Kimberly KENNER Lukas MERKEL Olaf LOOK A Thomas ABRAHAM Brian J ZIMMERMAN Mark W

Rok publikování 2024
Druh Článek v odborném periodiku
Časopis / Zdroj CELL REPORTS MEDICINE
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S2666379124001186?via%3Dihub
Doi http://dx.doi.org/10.1016/j.xcrm.2024.101472
Klíčová slova anaplastic large cell lymphoma; STAT3
Přiložené soubory
Popis Anaplastic large cell lymphoma (ALCL) is an aggressive, CD30 + T cell lymphoma of children and adults. ALK fusion transcripts or mutations in the JAK-STAT pathway are observed in most ALCL tumors, but the mechanisms underlying tumorigenesis are not fully understood. Here, we show that dysregulated STAT3 in ALCL cooccupies enhancers with master transcription factors BATF3, IRF4, and IKZF1 to form a core regulatory circuit that establishes and maintains the malignant cell state in ALCL. Critical downstream targets of this network in ALCL cells include the protooncogene MYC , which requires active STAT3 to facilitate high levels of MYC transcription. The core autoregulatory transcriptional circuitry activity is reinforced by MYC binding to the enhancer regions associated with STAT3 and each of the core regulatory transcription factors. Thus, activation of STAT3 provides the crucial link between aberrant tyrosine kinase signaling and the core transcriptional machinery that drives tumorigenesis and creates therapeutic vulnerabilities in ALCL.
Související projekty:

Používáte starou verzi internetového prohlížeče. Doporučujeme aktualizovat Váš prohlížeč na nejnovější verzi.

Další info