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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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 |
work_keys_str_mv |
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