Extracellular vesicles from non-neuroendocrine SCLC cells promote adhesion and survival of neuroendocrine SCLC cells

Abstract

Small Cell Lung Cancer (SCLC) tumors are made up of distinct cell subpopulations, including neuroendocrine (NE) and non-NE cells. While secreted factors from non-NE SCLC cells have been shown to support the growth of the NE cells, the underlying molecular factors are not well understood. Here, we show that exosome-type small extracellular vesicles (SEVs) secreted from non-NE SCLC cells promote adhesion and survival of NE SCLC cells. Proteomic analysis of purified small EVs revealed that extracellular matrix (ECM) proteins and integrins are highly enriched in small EVs of non-NE cells whereas nucleic acid-binding proteins are enriched in small EVs purified from NE cells. Addition of select purified ECM proteins identified in purified EVs, specifically fibronectin, laminin 411, and laminin 511, were able to substitute for the role of non-NE-derived SEVs in promoting adhesion, survival, and tumorigenicity of NE SCLC cells. Those same proteins were differentially expressed by human SCLC subtypes. These data suggest that ECM-carrying SEVs secreted by non-NE cells play a key role in supporting SCLC tumor growth and survival.

Extracellular vesicles—An omics view

“…EVs are important complex signaling players in the tumor microenvironment, interacting not only with diverse cell types to regulate and alter their functions, but further in their dynamic interaction with the extracellular matrix (ECM). Jiminez identified specific cells could synthesize and secrete quantities of ECM that are carried primarily by small EVs [26]. The study identified that protein cargo associated small EVs comprised the ECM factors in cancer cells enhanced adhesion and survival of stem‐like, tumor propagating cells, where the ECM‐carrying EVs from cancer cells induce a morphological shift from cell‐cell to cell‐substrate adhesion.…”