Skip to main content
Erschienen in: Pathology & Oncology Research 1/2017

30.07.2016 | Original Article

Quantification of Circulating Free DNA as a Diagnostic Marker in Gall Bladder Cancer

verfasst von: Swati Kumari, Shikha Tewari, Nuzhat Husain, Akash Agarwal, Anshuman Pandey, Ashish Singhal, Mohtashim Lohani

Erschienen in: Pathology & Oncology Research | Ausgabe 1/2017

Einloggen, um Zugang zu erhalten

Abstract

Gall bladder Carcinoma (GBC) is the fifth most common cancer of the digestive tract and frequently diagnosed in late stage of disease. Estimation of circulating free DNA (cfDNA) in serum has been applied as a “liquid biopsy” in several deep seated malignancies. Its value in diagnosis of gall bladder carcinoma has not been studied. The present study was designed to assess the role of cfDNA in the diagnosis of GBC and correlate levels with the TNM stage. Serum was collected from 34 patients with GBC and 39 age and sex matched controls including 22 cholecystitis and 17 healthy individuals. Serum cfDNA levels were measured through quantitative polymerase chain reaction (qPCR) by amplification of β-globin gene. Performance of the assay was calculated through the receiver operating characteristic (ROC) curve. The cfDNA level was significantly lower in healthy controls and cholecystitis (89.32 ± 59.76 ng/ml, 174.21 ± 99.93 ng/ml) compared to GBC (1245.91 ± 892.46 ng/ml, p = <0.001). The cfDNA level was significantly associated with TNM stage, lymph node involvement and jaundice (0.002, 0.027, and 0.041, respectively). Area under curve of ROC analysis for cancer group versus healthy and cholecystitis group was 1.00 and 0.983 with sensitivity of 100 %, 88.24 % and specificity of 100 % respectively. Quantitative analysis of cfDNA may distinguish cholecystitis and gall bladder carcinoma and may serve as new diagnostic, noninvasive marker adjunct to imaging for the diagnosis of GBC.
Literatur
1.
Zurück zum Zitat Mishra S, Chaturvedi A, Mishra NC, Sharma ID (2013) Carcinoma of the gallbladder. The Lancet Oncology 4:167–176CrossRef Mishra S, Chaturvedi A, Mishra NC, Sharma ID (2013) Carcinoma of the gallbladder. The Lancet Oncology 4:167–176CrossRef
2.
Zurück zum Zitat Hamdani NS, Qadri SK, Aggarwalla R, Bhartia VK, Chaudhuri S, Debakshi S, Baig SJ, Pal NK (2013) Clinicopathological Study of Gall Bladder Carcinoma with Special Reference to Gallstones: Our 8-year Experience from Eastern India. Asian Pacific J Cancer Prev 13(11):5613–5617CrossRef Hamdani NS, Qadri SK, Aggarwalla R, Bhartia VK, Chaudhuri S, Debakshi S, Baig SJ, Pal NK (2013) Clinicopathological Study of Gall Bladder Carcinoma with Special Reference to Gallstones: Our 8-year Experience from Eastern India. Asian Pacific J Cancer Prev 13(11):5613–5617CrossRef
3.
Zurück zum Zitat Goldin RD, Roa JC (2009) Gallbladder cancer: a morphological and molecular update. Histopathology 55:218–229CrossRefPubMed Goldin RD, Roa JC (2009) Gallbladder cancer: a morphological and molecular update. Histopathology 55:218–229CrossRefPubMed
4.
Zurück zum Zitat Kapoor VK, Michael AJ Mc (2003) Gallbladder cancer: An ‘Indian’ disease. Natl Med J India 4:16. Kapoor VK, Michael AJ Mc (2003) Gallbladder cancer: An ‘Indian’ disease. Natl Med J India 4:16.
5.
Zurück zum Zitat Peng HH, Zhang YD, Gong LS, Liu WD, Zhang Y (2013) Increased expression of microRNA-335 predicts a favorable prognosis in primary gallbladder carcinoma. Onco Targets Ther 6:1625–1630. Peng HH, Zhang YD, Gong LS, Liu WD, Zhang Y (2013) Increased expression of microRNA-335 predicts a favorable prognosis in primary gallbladder carcinoma. Onco Targets Ther 6:1625–1630.
6.
Zurück zum Zitat Liu TY, Tan ZJ, Jiang L, JF G, XS W, Cao Y, Li ML, KJ W, Liu YB (2013) Curcumin induces apoptosis in gallbladder carcinoma cell line GBC-SD cells. Cancer Cell Int 13:6CrossRef Liu TY, Tan ZJ, Jiang L, JF G, XS W, Cao Y, Li ML, KJ W, Liu YB (2013) Curcumin induces apoptosis in gallbladder carcinoma cell line GBC-SD cells. Cancer Cell Int 13:6CrossRef
7.
Zurück zum Zitat Stroun M, Maurice P, Vasioukhin V, Lyautey J, Lederry C, Lefort F (2000) The origin and mechanism of circulating DNA. Ann N Y Acad Sci 906:161–168CrossRefPubMed Stroun M, Maurice P, Vasioukhin V, Lyautey J, Lederry C, Lefort F (2000) The origin and mechanism of circulating DNA. Ann N Y Acad Sci 906:161–168CrossRefPubMed
8.
Zurück zum Zitat Ellinger J, Bastian PJ, Haan KI, Heukamp LC, Buettner R, Fimmers R, Mueller SC, Von Ruecker A (2008) Noncancerous PTGS2 DNA fragments of apoptotic origin in sera of prostate cancer patients qualify as diagnostic and prognostic indicators. Int J Cancer 122(1):138–143CrossRefPubMed Ellinger J, Bastian PJ, Haan KI, Heukamp LC, Buettner R, Fimmers R, Mueller SC, Von Ruecker A (2008) Noncancerous PTGS2 DNA fragments of apoptotic origin in sera of prostate cancer patients qualify as diagnostic and prognostic indicators. Int J Cancer 122(1):138–143CrossRefPubMed
9.
Zurück zum Zitat Sozzi G, Conte D, Mariani L (2001) Analysis of circulating tumor DNA in plasma at diagnosis and during follow-up of lung cancer patients. Cancer Res 61:4675–4678PubMed Sozzi G, Conte D, Mariani L (2001) Analysis of circulating tumor DNA in plasma at diagnosis and during follow-up of lung cancer patients. Cancer Res 61:4675–4678PubMed
10.
Zurück zum Zitat Umetani N, Kim J, Hiramatsu S (2006) Increased integrity of free circulating DNA in sera of patients with colorectal or periampullary cancer: direct quantitative PCR for ALU repeats. Clin Chem 52:1062–1069. Umetani N, Kim J, Hiramatsu S (2006) Increased integrity of free circulating DNA in sera of patients with colorectal or periampullary cancer: direct quantitative PCR for ALU repeats. Clin Chem 52:1062–1069.
11.
Zurück zum Zitat Trejo-Becerril C, Perez-Cardenas E, Trevino-Cuevas H (2003) Circulating nucleosomes and response to chemotherapy: an in vitro, in vivo and clinical study on cervical cancer patients. Int J Cancer 104:663–668CrossRefPubMed Trejo-Becerril C, Perez-Cardenas E, Trevino-Cuevas H (2003) Circulating nucleosomes and response to chemotherapy: an in vitro, in vivo and clinical study on cervical cancer patients. Int J Cancer 104:663–668CrossRefPubMed
12.
Zurück zum Zitat Chang HW, Lee SM, Goodman SN (2002) Assessment of plasma DNA levels, allelic imbalance, and CA 125 as diagnostic tests for cancer. J Natl. Cancer Inst 94:1697–1703CrossRefPubMed Chang HW, Lee SM, Goodman SN (2002) Assessment of plasma DNA levels, allelic imbalance, and CA 125 as diagnostic tests for cancer. J Natl. Cancer Inst 94:1697–1703CrossRefPubMed
13.
Zurück zum Zitat Gal S, Fidler C, Lo YMD, Taylor M, Han C, Moore J, Harris AL, Wainscoat JS (2004) Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR. Br J Cancer 90:1211–1215CrossRefPubMedPubMedCentral Gal S, Fidler C, Lo YMD, Taylor M, Han C, Moore J, Harris AL, Wainscoat JS (2004) Quantitation of circulating DNA in the serum of breast cancer patients by real-time PCR. Br J Cancer 90:1211–1215CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Ellinger J, Wittkamp V, Albers P (2009) Cell-free circulating DNA: diagnostic value in patients with testicular germ cell cancer. J Urol 181:363–371CrossRefPubMed Ellinger J, Wittkamp V, Albers P (2009) Cell-free circulating DNA: diagnostic value in patients with testicular germ cell cancer. J Urol 181:363–371CrossRefPubMed
15.
Zurück zum Zitat Ellinger J, Bastian PJ, Ellinger N (2008) Apoptotic DNA fragments in serum of patients with muscle invasive bladder cancer: a prognostic entity. Cancer Lett 264:274–280CrossRefPubMed Ellinger J, Bastian PJ, Ellinger N (2008) Apoptotic DNA fragments in serum of patients with muscle invasive bladder cancer: a prognostic entity. Cancer Lett 264:274–280CrossRefPubMed
16.
Zurück zum Zitat Altimari A, Grigioni AD, Benedettini E (2008) Diagnostic role of circulating free plasma DNA detection in patients with localized prostate cancer. Am. J Clin Pathol 129:756–762CrossRefPubMed Altimari A, Grigioni AD, Benedettini E (2008) Diagnostic role of circulating free plasma DNA detection in patients with localized prostate cancer. Am. J Clin Pathol 129:756–762CrossRefPubMed
17.
Zurück zum Zitat Sai S, Ichikawa D, Tomita H, Ikoma D, Tani N, Ikoma H, Kikuchi S, Fujiwara H, Ueda Y, Otsuji E (2007) Quantification of Plasma Cell-free DNA in Patients with Gastric Cancer. Anticancer Res 27:2747–2752PubMed Sai S, Ichikawa D, Tomita H, Ikoma D, Tani N, Ikoma H, Kikuchi S, Fujiwara H, Ueda Y, Otsuji E (2007) Quantification of Plasma Cell-free DNA in Patients with Gastric Cancer. Anticancer Res 27:2747–2752PubMed
18.
Zurück zum Zitat Chen K, Zhang H, Zhang L, SQ J, Qi J, Huang DF, Li F, Wei Q, Jing Zhang J (2013) Value of circulating cell-free DNA in diagnosis of hepatocellular carcinoma. World J Gastroenterol 19(20):3143–3149CrossRefPubMedPubMedCentral Chen K, Zhang H, Zhang L, SQ J, Qi J, Huang DF, Li F, Wei Q, Jing Zhang J (2013) Value of circulating cell-free DNA in diagnosis of hepatocellular carcinoma. World J Gastroenterol 19(20):3143–3149CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Lo YMD, Rainer TH, Chan LYS, Hjelm NM, Cocks RA (2000) Plasma DNA as a Prognostic Marker in Trauma Patients. Clin Chem 46(3):319–323PubMed Lo YMD, Rainer TH, Chan LYS, Hjelm NM, Cocks RA (2000) Plasma DNA as a Prognostic Marker in Trauma Patients. Clin Chem 46(3):319–323PubMed
20.
Zurück zum Zitat Ghosh M, Sakhuja P, Singh S, Agarwal AK (2013) p53 and beta catenin expression in gallbladder tissues and correlation with tumor progression in gallbladder cancer. Saudi J Gastroenterol 19:34–39CrossRefPubMedPubMedCentral Ghosh M, Sakhuja P, Singh S, Agarwal AK (2013) p53 and beta catenin expression in gallbladder tissues and correlation with tumor progression in gallbladder cancer. Saudi J Gastroenterol 19:34–39CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat He CZ, Zhang KH, Li Q, Liu XH, Hong Y, Lv NH (2013) Combined use of AFP, CEA, CA125 and CAl9–9 improves the sensitivity for the diagnosis of gastric cancer. BMC Gastroenterol 13:87. He CZ, Zhang KH, Li Q, Liu XH, Hong Y, Lv NH (2013) Combined use of AFP, CEA, CA125 and CAl9–9 improves the sensitivity for the diagnosis of gastric cancer. BMC Gastroenterol 13:87.
22.
Zurück zum Zitat Zhang D, Yu M, Xu T, Xiong B (2013) Predictive value of serum CEA, CA19–9 and CA125 in diagnosis of colorectal liver metastasis in Chinese population. Hepato-Gastroenterology 60:1297–1301PubMed Zhang D, Yu M, Xu T, Xiong B (2013) Predictive value of serum CEA, CA19–9 and CA125 in diagnosis of colorectal liver metastasis in Chinese population. Hepato-Gastroenterology 60:1297–1301PubMed
23.
Zurück zum Zitat Nath A, Kumar S, Singh M, Nadeem T, Murti K, Gupta AK, Das P, Kumar A (2015) Combined assessment of lipid peroxidation, Cea and Ca19.9 biomarkers in advanced stage gall bladder cancer. Int J Recent Sci Res 6::3136–3314 Nath A, Kumar S, Singh M, Nadeem T, Murti K, Gupta AK, Das P, Kumar A (2015) Combined assessment of lipid peroxidation, Cea and Ca19.9 biomarkers in advanced stage gall bladder cancer. Int J Recent Sci Res 6::3136–3314
24.
Zurück zum Zitat Leon SA, Shapiro B, Sklaroff DM, Yaros MJ (1977) Free DNA in the serum of cancer patients and the effect of therapy. Cancer Res 37:646–650PubMed Leon SA, Shapiro B, Sklaroff DM, Yaros MJ (1977) Free DNA in the serum of cancer patients and the effect of therapy. Cancer Res 37:646–650PubMed
25.
Zurück zum Zitat Umetani N, Hiramatsu S, Hoon DSB (2006) Higher amount of free circulating DNA in serum than in plasma is not mainly caused by contaminated extraneous DNA during separation. Annals NY Acad Sci 1075:299–307CrossRef Umetani N, Hiramatsu S, Hoon DSB (2006) Higher amount of free circulating DNA in serum than in plasma is not mainly caused by contaminated extraneous DNA during separation. Annals NY Acad Sci 1075:299–307CrossRef
26.
Zurück zum Zitat Gormally E, Caboux E, Vineis P, Hainaut P (2007) Circulating free DNA in plasma or serum as biomarker of carcinogenesis: Practical aspects and biological significance. Mutat Res 635:105–117CrossRefPubMed Gormally E, Caboux E, Vineis P, Hainaut P (2007) Circulating free DNA in plasma or serum as biomarker of carcinogenesis: Practical aspects and biological significance. Mutat Res 635:105–117CrossRefPubMed
27.
Zurück zum Zitat Pinzani P, Salvianti F, Pazzagli M, Orlando C (2010) Circulating nucleic acids in cancer and pregnancy. Methods 50:302–307CrossRefPubMed Pinzani P, Salvianti F, Pazzagli M, Orlando C (2010) Circulating nucleic acids in cancer and pregnancy. Methods 50:302–307CrossRefPubMed
28.
Zurück zum Zitat Swarup V, Rajeswari MR (2007) Circulating (cell-free) nucleic acids – a promising, Non-invasive tool for early detection of several human diseases. FEBS Lett 581:795–799CrossRefPubMed Swarup V, Rajeswari MR (2007) Circulating (cell-free) nucleic acids – a promising, Non-invasive tool for early detection of several human diseases. FEBS Lett 581:795–799CrossRefPubMed
Metadaten
Titel
Quantification of Circulating Free DNA as a Diagnostic Marker in Gall Bladder Cancer
verfasst von
Swati Kumari
Shikha Tewari
Nuzhat Husain
Akash Agarwal
Anshuman Pandey
Ashish Singhal
Mohtashim Lohani
Publikationsdatum
30.07.2016
Verlag
Springer Netherlands
Erschienen in
Pathology & Oncology Research / Ausgabe 1/2017
Print ISSN: 1219-4956
Elektronische ISSN: 1532-2807
DOI
https://doi.org/10.1007/s12253-016-0087-0

Weitere Artikel der Ausgabe 1/2017

Pathology & Oncology Research 1/2017 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.