Challenges for Better Diagnosis and Management of Pancreatic and Biliary Tract Cancers Focusing on Blood Biomarkers: A Systematic Review
Background: pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addit...
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Published in | Cancers Vol. 13; no. 16; p. 4220 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
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23.08.2021
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Online Access | Get full text |
ISSN | 2072-6694 2072-6694 |
DOI | 10.3390/cancers13164220 |
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Abstract | Background: pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addition, genetic abnormalities occur in cancer tissues, which ultimately affect the expression of various molecules. Therefore, it is important to identify molecules that are altered in PCa and BTC. For this systematic review, a systematic review of Medline and Embase to select biomarker studies of PCa and BTC patients was conducted. Results: after reviewing 72 studies, 79 biomarker candidates were identified, including 22 nucleic acids, 43 proteins, and 14 immune cell types. Of the 72 studies, 61 examined PCa, and 11 examined BTC. Conclusion: PCa and BTC are characterized by nucleic acid, protein, and immune cell profiles that are markedly different from those of healthy subjects. These altered molecules and cell subsets may serve as cancer-specific biomarkers, particularly in blood. Further studies are needed to better understand the diagnosis and prognosis of PCa and BTC. |
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AbstractList | Simple SummaryPancreatic and biliary tract cancers are malignant tumors that have a very poor prognosis and are resistant to chemotherapy. The later a cancer is detected, the worse the prognosis becomes; therefore, early detection is important. Biomarkers are physiological indices that serve as a guide to indicate the presence or absence of a certain disease, or its progression. The purpose of our research is to summarize previously reported biomarkers for the diagnosis and prognosis of pancreatic and biliary tract cancers. AbstractBackground: pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addition, genetic abnormalities occur in cancer tissues, which ultimately affect the expression of various molecules. Therefore, it is important to identify molecules that are altered in PCa and BTC. For this systematic review, a systematic review of Medline and Embase to select biomarker studies of PCa and BTC patients was conducted. Results: after reviewing 72 studies, 79 biomarker candidates were identified, including 22 nucleic acids, 43 proteins, and 14 immune cell types. Of the 72 studies, 61 examined PCa, and 11 examined BTC. Conclusion: PCa and BTC are characterized by nucleic acid, protein, and immune cell profiles that are markedly different from those of healthy subjects. These altered molecules and cell subsets may serve as cancer-specific biomarkers, particularly in blood. Further studies are needed to better understand the diagnosis and prognosis of PCa and BTC. pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addition, genetic abnormalities occur in cancer tissues, which ultimately affect the expression of various molecules. Therefore, it is important to identify molecules that are altered in PCa and BTC. For this systematic review, a systematic review of Medline and Embase to select biomarker studies of PCa and BTC patients was conducted.BACKGROUNDpancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addition, genetic abnormalities occur in cancer tissues, which ultimately affect the expression of various molecules. Therefore, it is important to identify molecules that are altered in PCa and BTC. For this systematic review, a systematic review of Medline and Embase to select biomarker studies of PCa and BTC patients was conducted.after reviewing 72 studies, 79 biomarker candidates were identified, including 22 nucleic acids, 43 proteins, and 14 immune cell types. Of the 72 studies, 61 examined PCa, and 11 examined BTC.RESULTSafter reviewing 72 studies, 79 biomarker candidates were identified, including 22 nucleic acids, 43 proteins, and 14 immune cell types. Of the 72 studies, 61 examined PCa, and 11 examined BTC.PCa and BTC are characterized by nucleic acid, protein, and immune cell profiles that are markedly different from those of healthy subjects. These altered molecules and cell subsets may serve as cancer-specific biomarkers, particularly in blood. Further studies are needed to better understand the diagnosis and prognosis of PCa and BTC.CONCLUSIONPCa and BTC are characterized by nucleic acid, protein, and immune cell profiles that are markedly different from those of healthy subjects. These altered molecules and cell subsets may serve as cancer-specific biomarkers, particularly in blood. Further studies are needed to better understand the diagnosis and prognosis of PCa and BTC. Background: pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late detection. Many researchers are tackling to develop non-invasive biomarkers for cancer, but few are specific for PCa or BTC. In addition, genetic abnormalities occur in cancer tissues, which ultimately affect the expression of various molecules. Therefore, it is important to identify molecules that are altered in PCa and BTC. For this systematic review, a systematic review of Medline and Embase to select biomarker studies of PCa and BTC patients was conducted. Results: after reviewing 72 studies, 79 biomarker candidates were identified, including 22 nucleic acids, 43 proteins, and 14 immune cell types. Of the 72 studies, 61 examined PCa, and 11 examined BTC. Conclusion: PCa and BTC are characterized by nucleic acid, protein, and immune cell profiles that are markedly different from those of healthy subjects. These altered molecules and cell subsets may serve as cancer-specific biomarkers, particularly in blood. Further studies are needed to better understand the diagnosis and prognosis of PCa and BTC. |
Author | Manabe, Haruki Yokoyama, Riko Saito, Yoshimasa Shimamura, Atsushi Serizawa, Yusuke Tominaga, Hiroto Oikawa, Chihiro Ochiya, Takahiro Toyoshima, Kensho Matsuzaki, Juntaro Ozawa, Eriko |
AuthorAffiliation | 1 Division of Pharmacotherapeutics, Keio University Faculty of Pharmacy, 1-5-30 Shibakoen, Minato-ku, Tokyo 105-8512, Japan; tominagahiroto@keio.jp (H.T.); 0808oocc@keio.jp (C.O.); toyoken724@keio.jp (K.T.); haruki.may19@keio.jp (H.M.); eriko.ozw@gmail.com (E.O.); btw.orz.321427@keio.jp (A.S.); rikoy@keio.jp (R.Y.); serizawa.y29@keio.jp (Y.S.) 2 Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan; tochiya@tokyo-med.ac.jp |
AuthorAffiliation_xml | – name: 1 Division of Pharmacotherapeutics, Keio University Faculty of Pharmacy, 1-5-30 Shibakoen, Minato-ku, Tokyo 105-8512, Japan; tominagahiroto@keio.jp (H.T.); 0808oocc@keio.jp (C.O.); toyoken724@keio.jp (K.T.); haruki.may19@keio.jp (H.M.); eriko.ozw@gmail.com (E.O.); btw.orz.321427@keio.jp (A.S.); rikoy@keio.jp (R.Y.); serizawa.y29@keio.jp (Y.S.) – name: 2 Department of Molecular and Cellular Medicine, Institute of Medical Science, Tokyo Medical University, 6-7-1 Nishishinjuku, Shinjuku-ku, Tokyo 160-0023, Japan; tochiya@tokyo-med.ac.jp |
Author_xml | – sequence: 1 givenname: Hiroto surname: Tominaga fullname: Tominaga, Hiroto – sequence: 2 givenname: Juntaro orcidid: 0000-0002-3204-5049 surname: Matsuzaki fullname: Matsuzaki, Juntaro – sequence: 3 givenname: Chihiro surname: Oikawa fullname: Oikawa, Chihiro – sequence: 4 givenname: Kensho surname: Toyoshima fullname: Toyoshima, Kensho – sequence: 5 givenname: Haruki surname: Manabe fullname: Manabe, Haruki – sequence: 6 givenname: Eriko surname: Ozawa fullname: Ozawa, Eriko – sequence: 7 givenname: Atsushi surname: Shimamura fullname: Shimamura, Atsushi – sequence: 8 givenname: Riko surname: Yokoyama fullname: Yokoyama, Riko – sequence: 9 givenname: Yusuke surname: Serizawa fullname: Serizawa, Yusuke – sequence: 10 givenname: Takahiro surname: Ochiya fullname: Ochiya, Takahiro – sequence: 11 givenname: Yoshimasa surname: Saito fullname: Saito, Yoshimasa |
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Snippet | Background: pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this... Simple SummaryPancreatic and biliary tract cancers are malignant tumors that have a very poor prognosis and are resistant to chemotherapy. The later a cancer... pancreatic cancer (PCa) and biliary tract cancer (BTC) are cancers with a poor prognosis and few effective treatments. One of the reasons for this is late... |
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SubjectTerms | Antigens Biliary tract Biomarkers Cancer therapies Chemotherapy Cholangiocarcinoma Diagnosis Fibroblasts Lymphocytes Medical prognosis Metastasis MicroRNAs Neuroendocrine tumors Pancreatic cancer Plasma Prognosis Protein expression Proteins Review Systematic review Tumors |
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Title | Challenges for Better Diagnosis and Management of Pancreatic and Biliary Tract Cancers Focusing on Blood Biomarkers: A Systematic Review |
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