Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway

Abstract Background Elevated lactate results in an acidic tumor microenvironment (TME), which stimulates the progression of esophageal cancer (EC). Tumor‐associated macrophages (TAMs) are an essential component of the TME. However, the regulatory mechanisms of lactate secreted by EC on TAMs and the...

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Main Authors: Chunsheng Zhang, Wei Cheng, Tongjin Yang, Hanlin Fang, Renquan Zhang
Format: Article
Language:English
Published: Wiley 2023-08-01
Series:Thoracic Cancer
Subjects:
Online Access:https://doi.org/10.1111/1759-7714.14998
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author Chunsheng Zhang
Wei Cheng
Tongjin Yang
Hanlin Fang
Renquan Zhang
author_facet Chunsheng Zhang
Wei Cheng
Tongjin Yang
Hanlin Fang
Renquan Zhang
author_sort Chunsheng Zhang
collection DOAJ
description Abstract Background Elevated lactate results in an acidic tumor microenvironment (TME), which stimulates the progression of esophageal cancer (EC). Tumor‐associated macrophages (TAMs) are an essential component of the TME. However, the regulatory mechanisms of lactate secreted by EC on TAMs and the effects of EC advancement are unclear. Methods Proteins and mRNA expression were determined by western blot and RT‐qPCR. Cell metastasis and growth were assessed by scratch assay, transwell and BrdU assays. Lactate in cells was quantified using a lactate kit. A mouse model was constructed for validation in vivo. Results First, we determined that lactate upgraded the M2‐type polarization marker levels of macrophages. Cell function assays confirmed that lactate‐activated M2 macrophages accelerated EC cell migration and proliferation in vitro. However, the lactate inhibitor – oxamate hampered the level of lactate in TE‐1 cells. Oxamate abolished the facilitation of macrophage polarization by lactate. In addition, we discovered that phosphorylated AKT and phosphorylated ERK was obviously raised in lactate‐stimulated macrophages, and oxamate addition reversed this change, implying that AKT and ERK signaling pathways were involved in macrophage polarization. Response experiments proved that attenuation of AKT/ERK signaling markedly returned the lactate‐induced promotion of EC migration and proliferation by macrophages. Finally, mouse tumor models demonstrated that lactate enhanced EC growth by inducing M2 macrophage polarization. Conclusion EC‐secreted lactate stimulated macrophage M2 polarization via the AKT/ERK pathway thereby boosting the growth of EC.
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spelling doaj.art-aa03a119952842b28b75db36059aa5e22023-08-03T01:12:13ZengWileyThoracic Cancer1759-77061759-77142023-08-0114222139214810.1111/1759-7714.14998Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathwayChunsheng Zhang0Wei Cheng1Tongjin Yang2Hanlin Fang3Renquan Zhang4Department of Thoracic Surgery First Affiliated Hospital of Anhui Medical University Hefei ChinaDepartment of Radiotherapy Luan Hospital of Chinese Medicine affiliated to Anhui University of Chinese Medicine Luan ChinaLaboratory of Toxicology, Anhui Provincial Center for Disease Control and Prevention Hefei ChinaDepartment of Thoracic Surgery First Affiliated Hospital of Anhui Medical University Hefei ChinaDepartment of Thoracic Surgery First Affiliated Hospital of Anhui Medical University Hefei ChinaAbstract Background Elevated lactate results in an acidic tumor microenvironment (TME), which stimulates the progression of esophageal cancer (EC). Tumor‐associated macrophages (TAMs) are an essential component of the TME. However, the regulatory mechanisms of lactate secreted by EC on TAMs and the effects of EC advancement are unclear. Methods Proteins and mRNA expression were determined by western blot and RT‐qPCR. Cell metastasis and growth were assessed by scratch assay, transwell and BrdU assays. Lactate in cells was quantified using a lactate kit. A mouse model was constructed for validation in vivo. Results First, we determined that lactate upgraded the M2‐type polarization marker levels of macrophages. Cell function assays confirmed that lactate‐activated M2 macrophages accelerated EC cell migration and proliferation in vitro. However, the lactate inhibitor – oxamate hampered the level of lactate in TE‐1 cells. Oxamate abolished the facilitation of macrophage polarization by lactate. In addition, we discovered that phosphorylated AKT and phosphorylated ERK was obviously raised in lactate‐stimulated macrophages, and oxamate addition reversed this change, implying that AKT and ERK signaling pathways were involved in macrophage polarization. Response experiments proved that attenuation of AKT/ERK signaling markedly returned the lactate‐induced promotion of EC migration and proliferation by macrophages. Finally, mouse tumor models demonstrated that lactate enhanced EC growth by inducing M2 macrophage polarization. Conclusion EC‐secreted lactate stimulated macrophage M2 polarization via the AKT/ERK pathway thereby boosting the growth of EC.https://doi.org/10.1111/1759-7714.14998AKTECERKlactateM2 macrophages
spellingShingle Chunsheng Zhang
Wei Cheng
Tongjin Yang
Hanlin Fang
Renquan Zhang
Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
Thoracic Cancer
AKT
EC
ERK
lactate
M2 macrophages
title Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
title_full Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
title_fullStr Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
title_full_unstemmed Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
title_short Lactate secreted by esophageal cancer cells induces M2 macrophage polarization via the AKT/ERK pathway
title_sort lactate secreted by esophageal cancer cells induces m2 macrophage polarization via the akt erk pathway
topic AKT
EC
ERK
lactate
M2 macrophages
url https://doi.org/10.1111/1759-7714.14998
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