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. Author manuscript; available in PMC: 2018 Jun 12.
Published in final edited form as: Nat Biomed Eng. 2017 Dec 12;1:993–1003. doi: 10.1038/s41551-017-0167-9

Table 1. Distinct metastatic lesions originating from a common cell line exhibit niche-dependent molecular signatures.

Cancerous cells isolated from adrenal and bones were cultured ex vivo and analyzed for changes in biomarker expression with a hematopoietic array. Cellular markers upregulated in adrenal-tropic lines were typically associated with increased tumor growth and invasion, while those upregulated in the bone-tropic line act to promote bone resorption

PROTEINS UPREGULATED IN ADRENAL-TROPIC MCF7-6124A CELLS
Protein Fold Change Pathway activated Clinical relevance
N-Cadherin 4.75 Sustains activation of ERK and activates MMP-9 production Promotes invasive activity and increases tumor metastasis
ADAM17 6.5 Activates EGFR-MEK-ERK pathway and upregulates MMP-2 and MMP-9, stimulates the release of TGFα Increases cellular invasion and proliferation
JAM-A 4.5 Activates Rap1 GTPase and upregulates β1-integrin Increases cell motility
Indicates poor patient prognosis
PROTEINS UPREGULATED IN BONE-TROPIC MCF7-5624A CELLS
Notch-1 2 Activated by downstream products of TGFβ-SMAD pathway to promote osteoclast differentiation in bone Promotes bone reabsorption and osteolytic lesions
Amphiregulin 2 Stimulates and increases EGFR signaling Important for bone colonization
EGFR 2.27 Activation with MMP-1 leads to reduced production of osteoprotegrin, increasing RANKL activation of osteoclasts Impacts recruitment of osteoblasts, limiting bone mineralization