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PDCD4 is a CSL associated protein with a transcription repressive function in cancer associated fibroblast activation

Authors: Jo, Seung-Hee; Kim, Dong Eun; Dotto, G. Paolo; Clocchiatti, Andrea;

PDCD4 is a CSL associated protein with a transcription repressive function in cancer associated fibroblast activation

Abstract

The Notch/CSL pathway plays an important role in skin homeostasis and carcinogenesis. CSL, the key effector of canonical Notch signaling endowed with an intrinsic transcription repressive function, suppresses stromal fibroblast senescence and Cancer Associated Fibroblast (CAF) activation through direct down-modulation of key effector genes. Interacting proteins that participate with CSL in this context are as yet to be identified. We report here that Programmed Cell Death 4 (PDCD4), a nuclear/cytoplasmic shuttling protein with multiple functions, associates with CSL and plays a similar role in suppressing dermal fibroblast senescence and CAF activation. Like CSL, PDCD4 is down-regulated in stromal fibroblasts of premalignant skin actinic keratosis (AKs) lesions and squamous cell carcinoma (SCC). While devoid of intrinsic DNA binding capability, PDCD4 is present at CSL binding sites of CAF marker genes as well as canonical Notch/CSL targets and suppresses expression of these genes in a fibroblast-specific manner. Thus, we propose that PDCD4 is part of the CSL repressive complex involved in negative control of stromal fibroblasts conversion into CAFs.

Keywords

Skin Neoplasms, Transcription, Genetic, 610, Down-Regulation, Mice, SCID, squamous cancer, Mice, Animals; Apoptosis Regulatory Proteins/genetics; Apoptosis Regulatory Proteins/metabolism; Cancer-Associated Fibroblasts/immunology; Cancer-Associated Fibroblasts/metabolism; Carcinoma, Squamous Cell/genetics; Carcinoma, Squamous Cell/metabolism; Cell Line, Tumor; Cellular Senescence; Down-Regulation; HEK293 Cells; HeLa Cells; Humans; Immunoglobulin J Recombination Signal Sequence-Binding Protein/metabolism; Keratosis, Actinic/genetics; Keratosis, Actinic/metabolism; Mice; Mice, SCID; Protein Binding; RNA, Small Interfering/genetics; RNA-Binding Proteins/genetics; RNA-Binding Proteins/metabolism; Signal Transduction; Skin Neoplasms/genetics; Skin Neoplasms/metabolism; Transcription, Genetic; Xenograft Model Antitumor Assays; CAFs; Notch/CSL signaling; PDCD4; squamous cancer; transcription repression, Cancer-Associated Fibroblasts, Cell Line, Tumor, Animals, Humans, RNA, Small Interfering, Cellular Senescence, Notch/CSL signaling, PDCD4, CAFs, RNA-Binding Proteins, transcription repression, Keratosis, Actinic, HEK293 Cells, Immunoglobulin J Recombination Signal Sequence-Binding Protein, Carcinoma, Squamous Cell, Apoptosis Regulatory Proteins, Priority Research Paper, HeLa Cells, Protein Binding, Signal Transduction

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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    13
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Average
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
13
Top 10%
Average
Top 10%
Green
gold