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Targeting the Microenvironment in Esophageal Cancer

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TLDR
In this article, the authors summarized the microenvironment of esophageal cancer and the latest advances in microenvironment-targeting therapies in this review, and showed that TME is an important therapeutic target for EC and that many new drugs and therapies that have been developed to target microenvironment may become treatment options in the future.
Abstract
Esophageal cancer (EC) is the eighth most common type of cancer and the sixth leading cause of cancer-related deaths worldwide. At present, the clinical treatment for EC is based mainly on radical surgery, chemotherapy, and radiotherapy. However, due to the limited efficacy of conventional treatments and the serious adverse reactions, the outcome is still unsatisfactory (the 5-year survival rate for patients is less than 25%). Thus, it is extremely important and urgent to identify new therapeutic targets. The concept of tumor microenvironment (TME) has attracted increased attention since it was proposed. Recent studies have shown that TME is an important therapeutic target for EC. Microenvironment-targeting therapies such as immunotherapy and antiangiogenic therapy have played an indispensable role in prolonging survival and improving the prognosis of patients with EC. In addition, many new drugs and therapies that have been developed to target microenvironment may become treatment options in the future. We summarize the microenvironment of EC and the latest advances in microenvironment-targeting therapies in this review.

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Journal ArticleDOI

IGFBP7 remodels the tumor microenvironment of esophageal squamous cell carcinoma by activating the TGFβ1/SMAD signaling pathway

TL;DR: Increased IGFBP7 may accelerate the progression of ESCC by upregulating TGF β1, α-SMA, and collagen I via activating the TGFβ1/SMAD signaling pathway, which could remodel the TME.
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The Role of Tumor Microenvironment in Invasion and Metastasis of Esophageal Squamous Cell Carcinoma

TL;DR: This review will focus on the mechanism of different microenvironment cellular elements in ESCC invasion and metastasis and discuss recent therapeutic attempts to restore the tumor-suppressing function of cells within the TME.
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MAIP1-Related Tumor Immune Infiltration: As a Potential Prognostic Biomarker for Esophageal Cancer

TL;DR: It is proposed that MAIP1 overexpression was associated with poor prognosis and tumor immune infiltration in EC and further investigation is needed.
Journal ArticleDOI

Development and validation of a nomogram for patients with stage II/III gastric adenocarcinoma after radical surgery

TL;DR: Wang et al. as mentioned in this paper constructed nomograms based on clinicopathological features and routine preoperative hematological indices to predict cancer-specific survival (CSS) and disease-free survival (DFS) in patients with stage II/III gastric adenocarcinoma (GA) after radical resection.
References
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Journal ArticleDOI

Effect of curcumin on acidic pH-induced expression of IL-6 and IL-8 in human esophageal epithelial cells (HET-1A): role of PKC, MAPKs, and NF-κB

TL;DR: IL-6 and IL-8 expression by acid may contribute to the pathobiology of mucosal injury in GERD, and inhibition of the NF-kappaB/proinflammatory cytokine pathways may emerge as important therapeutic targets for treatment of esophageal inflammation.
Journal ArticleDOI

The Function of the HGF/c-Met Axis in Hepatocellular Carcinoma.

TL;DR: The HGF/c-Met axis promotes the onset, proliferation, invasion, and metastasis of HCC, and can serve as a biomarker for diagnosis and prognosis, as well as a therapeutic target for HCC.
Journal ArticleDOI

A Randomized Phase II Study of FOLFOX With or Without the MET Inhibitor Onartuzumab in Advanced Adenocarcinoma of the Stomach and Gastroesophageal Junction

TL;DR: The addition of onartuzumab to mFOLFOX6 in gastric cancer did not improve efficacy in an unselected population or in a MET immunohistochemistry-positive population, highlighting the importance of correctly selecting biomarkers for targeted therapies.
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