Circulating microRNAs as diagnostic and therapeutic biomarkers in gastric and esophageal cancers

Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarke...

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Published inJournal of cellular physiology Vol. 233; no. 11; pp. 8538 - 8550
Main Authors Jamali, Leila, Tofigh, Roghayeh, Tutunchi, Sara, Panahi, Ghodratollah, Borhani, Fatemeh, Akhavan, Saeedeh, Nourmohammadi, Parisa, Ghaderian, Sayyed M.H., Rasouli, Milad, Mirzaei, Hamed
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.11.2018
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Abstract Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarkers is a critical step in finding new approaches for the treatment of these cancers. Finding new biomarkers that cover various aspects of the diseases could provide a choice of suitable therapies and better monitoring of patients with these cancers. Among several biomarkers tissue specific and circulating microRNAs (miRNAs) have emerged as powerful candidates in the diagnosis of gastric and esophageal cancers. MiRNAs are small noncoding single‐stranded RNA molecules that are found in the blood and regulate gene expression. These have numerous characteristics that make them suitable for being used as ideal biomarkers in cancer diagnosis. Research has indicated that the level and profile of miRNA in serum and plasma are very high. They are potentially noninvasive and sensitive enough to detect tumors in their primary stages of infection. Multiple lines of evidence indicate that the presence, absence, or deregulation of several circulating miRNAs (i.e., let‐7a, miR‐21, miR‐93, miR‐192a, miR‐18a, and miR‐10b for gastric cancer, and miR‐21, miR‐375, miR‐25‐3p, miR‐151a‐3p, and miR‐100‐3p for esophageal cancer) are associated with initiation and progression of gastric and esophageal cancers. The aim of this review is to highlight the recent advances in the roles of miRNAs in diagnosis and treatment of gastric and esophageal cancers. The aims of this review is to highlight the recent advances in the roles of microRNAs in diagnosis and treatment of gastric and esophageal cancers.
AbstractList Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarkers is a critical step in finding new approaches for the treatment of these cancers. Finding new biomarkers that cover various aspects of the diseases could provide a choice of suitable therapies and better monitoring of patients with these cancers. Among several biomarkers tissue specific and circulating microRNAs (miRNAs) have emerged as powerful candidates in the diagnosis of gastric and esophageal cancers. MiRNAs are small noncoding single‐stranded RNA molecules that are found in the blood and regulate gene expression. These have numerous characteristics that make them suitable for being used as ideal biomarkers in cancer diagnosis. Research has indicated that the level and profile of miRNA in serum and plasma are very high. They are potentially noninvasive and sensitive enough to detect tumors in their primary stages of infection. Multiple lines of evidence indicate that the presence, absence, or deregulation of several circulating miRNAs (i.e., let‐7a, miR‐21, miR‐93, miR‐192a, miR‐18a, and miR‐10b for gastric cancer, and miR‐21, miR‐375, miR‐25‐3p, miR‐151a‐3p, and miR‐100‐3p for esophageal cancer) are associated with initiation and progression of gastric and esophageal cancers. The aim of this review is to highlight the recent advances in the roles of miRNAs in diagnosis and treatment of gastric and esophageal cancers.
Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarkers is a critical step in finding new approaches for the treatment of these cancers. Finding new biomarkers that cover various aspects of the diseases could provide a choice of suitable therapies and better monitoring of patients with these cancers. Among several biomarkers tissue specific and circulating microRNAs (miRNAs) have emerged as powerful candidates in the diagnosis of gastric and esophageal cancers. MiRNAs are small noncoding single‐stranded RNA molecules that are found in the blood and regulate gene expression. These have numerous characteristics that make them suitable for being used as ideal biomarkers in cancer diagnosis. Research has indicated that the level and profile of miRNA in serum and plasma are very high. They are potentially noninvasive and sensitive enough to detect tumors in their primary stages of infection. Multiple lines of evidence indicate that the presence, absence, or deregulation of several circulating miRNAs (i.e., let‐7a, miR‐21, miR‐93, miR‐192a, miR‐18a, and miR‐10b for gastric cancer, and miR‐21, miR‐375, miR‐25‐3p, miR‐151a‐3p, and miR‐100‐3p for esophageal cancer) are associated with initiation and progression of gastric and esophageal cancers. The aim of this review is to highlight the recent advances in the roles of miRNAs in diagnosis and treatment of gastric and esophageal cancers. The aims of this review is to highlight the recent advances in the roles of microRNAs in diagnosis and treatment of gastric and esophageal cancers.
Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarkers is a critical step in finding new approaches for the treatment of these cancers. Finding new biomarkers that cover various aspects of the diseases could provide a choice of suitable therapies and better monitoring of patients with these cancers. Among several biomarkers tissue specific and circulating microRNAs (miRNAs) have emerged as powerful candidates in the diagnosis of gastric and esophageal cancers. MiRNAs are small noncoding single-stranded RNA molecules that are found in the blood and regulate gene expression. These have numerous characteristics that make them suitable for being used as ideal biomarkers in cancer diagnosis. Research has indicated that the level and profile of miRNA in serum and plasma are very high. They are potentially noninvasive and sensitive enough to detect tumors in their primary stages of infection. Multiple lines of evidence indicate that the presence, absence, or deregulation of several circulating miRNAs (i.e., let-7a, miR-21, miR-93, miR-192a, miR-18a, and miR-10b for gastric cancer, and miR-21, miR-375, miR-25-3p, miR-151a-3p, and miR-100-3p for esophageal cancer) are associated with initiation and progression of gastric and esophageal cancers. The aim of this review is to highlight the recent advances in the roles of miRNAs in diagnosis and treatment of gastric and esophageal cancers.Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts were made in the past few decades to finding effective therapeutic approaches, but these approaches had several problems. Finding new biomarkers is a critical step in finding new approaches for the treatment of these cancers. Finding new biomarkers that cover various aspects of the diseases could provide a choice of suitable therapies and better monitoring of patients with these cancers. Among several biomarkers tissue specific and circulating microRNAs (miRNAs) have emerged as powerful candidates in the diagnosis of gastric and esophageal cancers. MiRNAs are small noncoding single-stranded RNA molecules that are found in the blood and regulate gene expression. These have numerous characteristics that make them suitable for being used as ideal biomarkers in cancer diagnosis. Research has indicated that the level and profile of miRNA in serum and plasma are very high. They are potentially noninvasive and sensitive enough to detect tumors in their primary stages of infection. Multiple lines of evidence indicate that the presence, absence, or deregulation of several circulating miRNAs (i.e., let-7a, miR-21, miR-93, miR-192a, miR-18a, and miR-10b for gastric cancer, and miR-21, miR-375, miR-25-3p, miR-151a-3p, and miR-100-3p for esophageal cancer) are associated with initiation and progression of gastric and esophageal cancers. The aim of this review is to highlight the recent advances in the roles of miRNAs in diagnosis and treatment of gastric and esophageal cancers.
Author Jamali, Leila
Panahi, Ghodratollah
Borhani, Fatemeh
Mirzaei, Hamed
Tutunchi, Sara
Rasouli, Milad
Tofigh, Roghayeh
Nourmohammadi, Parisa
Akhavan, Saeedeh
Ghaderian, Sayyed M.H.
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  surname: Jamali
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  organization: School of Medicine, Shahid Beheshti University of Medical Sciences
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  surname: Tofigh
  fullname: Tofigh, Roghayeh
  organization: Tabriz University
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  givenname: Sara
  surname: Tutunchi
  fullname: Tutunchi, Sara
  organization: Shahid Sadoughi University of Medical Sciences
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  givenname: Ghodratollah
  surname: Panahi
  fullname: Panahi, Ghodratollah
  organization: Faculty of Medicine, Tehran University of Medical Sciences
– sequence: 5
  givenname: Fatemeh
  surname: Borhani
  fullname: Borhani, Fatemeh
  organization: Faculty of Medicine, Shahid Beheshti University of Medical Sciences
– sequence: 6
  givenname: Saeedeh
  surname: Akhavan
  fullname: Akhavan, Saeedeh
  organization: School of Basic Sciences, Science and Research Branch, Islamic Azad University
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  surname: Nourmohammadi
  fullname: Nourmohammadi, Parisa
  organization: Shahid Sadoughi University of Medical Sciences
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  givenname: Sayyed M.H.
  surname: Ghaderian
  fullname: Ghaderian, Sayyed M.H.
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  organization: Shahid Beheshti University of Medical Sciences
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  surname: Rasouli
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  orcidid: 0000-0002-9399-8281
  surname: Mirzaei
  fullname: Mirzaei, Hamed
  email: h.mirzaei2002@gmail.com
  organization: Mashhad University of Medical Sciences
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ID FETCH-LOGICAL-c4190-7b32f867f47a4fa1cdb1411808cbf5245144180e030d88e7cec6df01d2a3e9ec3
IEDL.DBID DR2
ISSN 0021-9541
1097-4652
IngestDate Fri Jul 11 15:19:52 EDT 2025
Fri Jul 25 09:10:10 EDT 2025
Thu Apr 03 07:06:29 EDT 2025
Tue Jul 01 01:31:52 EDT 2025
Thu Apr 24 22:56:59 EDT 2025
Wed Jan 22 17:12:02 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 11
Keywords gastric carcinogenesis
microRNA (miRNA)
mechanisms
esophagal cancer
Language English
License 2018 Wiley Periodicals, Inc.
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MergedId FETCHMERGED-LOGICAL-c4190-7b32f867f47a4fa1cdb1411808cbf5245144180e030d88e7cec6df01d2a3e9ec3
Notes Ghaderian, Rasouli, and Mirzaei contributed equally to this work.
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content type line 14
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  text: November 2018
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– name: Hoboken
PublicationTitle Journal of cellular physiology
PublicationTitleAlternate J Cell Physiol
PublicationYear 2018
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Publisher_xml – name: Wiley Subscription Services, Inc
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Snippet Gastric and esophageal cancers are as main cancers of the gastrointestinal (GI) tract, which are associated with poor diagnosis and survival. Several efforts...
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SubjectTerms Biomarkers
Cancer
Deregulation
Diagnosis
Diagnostic systems
esophagal cancer
Esophageal cancer
Esophagus
Gastric cancer
gastric carcinogenesis
Gastrointestinal tract
Gene expression
mechanisms
microRNA (miRNA)
MicroRNAs
miRNA
Ribonucleic acid
RNA
Tumors
Title Circulating microRNAs as diagnostic and therapeutic biomarkers in gastric and esophageal cancers
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcp.26850
https://www.ncbi.nlm.nih.gov/pubmed/29923196
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