Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer

Together, gastric cancer and esophageal cancer (EC) possess two of the highest incidence rates amongst all cancers. They exhibit poor prognoses in which the 5-year survival rate is dismal. In addition to cytotoxic chemotherapy, treatment efforts have been geared toward targeting human epidermal grow...

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Main Authors: Ali Zubair Siddiqui, Khaldoun Almhanna
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/17/4322
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spelling doaj-494e68c6ae5346c49f7a19586674b23c2021-09-09T13:40:29ZengMDPI AGCancers2072-66942021-08-01134322432210.3390/cancers13174322Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal CancerAli Zubair Siddiqui0Khaldoun Almhanna1University of Mississippi Medical Center, University of Mississippi School of Medicine, Jackson, MS 39216, USAThe Brown University Oncology Research Group, The Rhode Island Hospital/Lifespan Cancer Institute, Providence, RI 02903, USATogether, gastric cancer and esophageal cancer (EC) possess two of the highest incidence rates amongst all cancers. They exhibit poor prognoses in which the 5-year survival rate is dismal. In addition to cytotoxic chemotherapy, treatment efforts have been geared toward targeting human epidermal growth factor receptor 2 (HER-2), vascular endothelial growth factor (VEGF), and programmed death ligand-1 (PD-1). Although ample success has been recorded with these agents, gastric and esophageal cancer remain lethal, and further research into potential treatment alternatives is needed. In this article, we will review some of the targets at the forefront of investigation such as claudin, Dickkopf-related protein 1 (DKK-1), fibroblast growth factor receptor (FGFR), and matrix metalloproteinases (MMPs). These innovative target pathways are in the midst of clinical trials to be implemented in the treatment algorithm for this patient population. Ultimately, exploiting the oncogenic tendencies of these potential biomarkers creates an opportunity for precise treatment and improved prognosis for these cancers. Lastly, research aimed toward reversing PD-1 antibodies resistance by combining it with other novel agents or other treatment modalities is underway in order to expand existing treatment options for this patient population.https://www.mdpi.com/2072-6694/13/17/4322gastric canceresophageal cancerclaudinDickkopf-related protein 1fibroblast growth factormatrix metalloproteinases
collection DOAJ
language English
format Article
sources DOAJ
author Ali Zubair Siddiqui
Khaldoun Almhanna
spellingShingle Ali Zubair Siddiqui
Khaldoun Almhanna
Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
Cancers
gastric cancer
esophageal cancer
claudin
Dickkopf-related protein 1
fibroblast growth factor
matrix metalloproteinases
author_facet Ali Zubair Siddiqui
Khaldoun Almhanna
author_sort Ali Zubair Siddiqui
title Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
title_short Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
title_full Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
title_fullStr Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
title_full_unstemmed Beyond Chemotherapy, PD-1, and HER-2: Novel Targets for Gastric and Esophageal Cancer
title_sort beyond chemotherapy, pd-1, and her-2: novel targets for gastric and esophageal cancer
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2021-08-01
description Together, gastric cancer and esophageal cancer (EC) possess two of the highest incidence rates amongst all cancers. They exhibit poor prognoses in which the 5-year survival rate is dismal. In addition to cytotoxic chemotherapy, treatment efforts have been geared toward targeting human epidermal growth factor receptor 2 (HER-2), vascular endothelial growth factor (VEGF), and programmed death ligand-1 (PD-1). Although ample success has been recorded with these agents, gastric and esophageal cancer remain lethal, and further research into potential treatment alternatives is needed. In this article, we will review some of the targets at the forefront of investigation such as claudin, Dickkopf-related protein 1 (DKK-1), fibroblast growth factor receptor (FGFR), and matrix metalloproteinases (MMPs). These innovative target pathways are in the midst of clinical trials to be implemented in the treatment algorithm for this patient population. Ultimately, exploiting the oncogenic tendencies of these potential biomarkers creates an opportunity for precise treatment and improved prognosis for these cancers. Lastly, research aimed toward reversing PD-1 antibodies resistance by combining it with other novel agents or other treatment modalities is underway in order to expand existing treatment options for this patient population.
topic gastric cancer
esophageal cancer
claudin
Dickkopf-related protein 1
fibroblast growth factor
matrix metalloproteinases
url https://www.mdpi.com/2072-6694/13/17/4322
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