BibTex RIS Kaynak Göster

Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study

Yıl 2016, Cilt: 2 Sayı: 3, 0 - 0, 29.09.2016

Öz

Background: There have been some relationship between Ki-67 and P53 expression and the standardized uptake value (SUVmax) of the primary lesion during
positron emission tomography-computed tomography (PET-CT) in lung cancers.
Methods: The staining density of Ki-67 and p53 expression in 31 cases were diagnosed with non-small cell carcinoma (NSLCL) and 13 cases were diagnosed with
small cell carcinoma (SCLC) have been investigated..
Results: Ki-67 % was significantly correlated with SUVmax values in patients with lung cancer in all subtypes (adenocarcinoma, squamous and small cell
lung cancer) but the regression analysis was more prominent in adenocarcinoma and squamous cell carcinoma. Squamous cell carcinoma group
had significantly correlated Ki 67 levels with overall survival (OS), and p53 levels had significantly correlated with progression free survival (PFS) and
OS. Adenocarcinoma and small cell lung carcinoma patients did not have any significant correlation between the Ki 67, p53 and OS as well as PFS.
Conclusions: There is a strong correlation between the SUVmax and pathologic staining of Ki 67 and p53. Squamous cell lung carcinoma subtype is highly expressed
p53 and Ki 67 with might predicted by SUVmax and these findings are significantly correlated with oncologic outcomes. .
Keywords: Ki 67, p53, SUV max, Lung cancer

Kaynakça

  • Siegel R, Ma J, Zou Z, and Jemal A . Cancer statistics. CA Cancer J Clin.2014;64:9-29.
  • Hillman GG, Lonardo F, Hoogstra DJ, Rakowski J, Yunker CK, Joiner MC,Dyson G, Gadgeel S, Singh-Gupta V. Axitinib Improves Radiotherapy inMurine Xenograft Lung Tumors. Transl Oncol. 2014;7:400-409.
  • Bilir C, Balık MS, Kızılkaya B, Yıldırım S, Gemez S, Bilir F. Serum LactateDehydrogenase Levels May Predict Fentanyl Usage in Patients withMetastatic Cancers for The Treatment of Cancer Related Pain. J hum
  • rhythm. 2016;2(2):78-82.
  • de Geus-Oei L, van Krieken JH, Aliredjo R, Krabbe PF, Frielink C, VerhagenAF, Boerman OC, Oyen WJ. Biological correlates of FDG uptake in nonsmallcell lung cancer. Lung Cancer. 2007; 55: 79–87.
  • Kieninger A, Welsh R, Bendick P, Zelenock G, Chmielewski GW. Positronemissiontomography as a prognostic tool for early-stage lung cancer. AmJ Surg. 2006; 191:433-436.
  • Vesselle H1, Schmidt RA, Pugsley JM, Li M, Kohlmyer SG, Vallires E, WoodDE. Lung cancer proliferation correlates with [F-18]fluorodeoxyglucoseuptake by positron emission tomography. Clin Cancer Res. 2000;6:3837-3844.
  • Higashi K1, Ito K, Hiramatsu Y, Ishikawa T, Sakuma T, Matsunari I, KugaG, Miura K, Higuchi T, Tonami H, Yamamoto I. 18F-FDG uptake by primarytumor as a predictor of intratumoral lymphatic vessel invasion and lymphnode involvement in non-small cell lung cancer: analysis of a multicenterstudy. J Nucl Med. 2005;46:267-273.
  • Zhang ZJ, Chen JH, Meng L, Du JJ, Zhang L, Liu Y, Dai HH. 18F-FDG uptakeas a biologic factor predicting outcome in patients with resected non-smallcelllung cancer. Chin Med J (Engl). 2007;120:125-131.
  • Jeong HJ, Min JJ, Park JM, Chung JK, Kim BT, Jeong JM, Lee DS, Lee
  • MC, Han SK, Shim YS. Determination of the prognostic value of [(18)F]
  • fluorodeoxyglucose uptake by using positron emission tomography in
  • patients with non-small cell lung cancer. 2002;23:865-870.
  • Viberti L, Papotti, M, Abbona G.C, Celano,A, Filosso PL, Bussolati G. Valueof Ki-67 immunostaining in preoperative biopsiesof carcinomas of the lung.Hum. Pathol.1997;28:189-192.
  • Minn H, Joensuu H, Ahonen A, Klemi P. Fluorodeoxyglucose imaging:
  • a method to assess the proliferative activity of human cancer in vivo.
  • Comparison with DNA flow cytometry in head and neck tumors. Cancer
  • (Phila.). 1988;61:1776–1781.
  • Haberkorn U, Strauss LG, Reisser C, Haag D, Dimitrakopoulou A, ZiglerS, Oberdorfer F, Rudat V, VanKaick G. Glucose uptake, perfusion, andcell proliferation in head and neck tumors: relation of positron emissiontomography to flow cytometry. J. Nucl.Med.1991;32: 1548-1555.
  • Lapela M, Leskinen S, Minn HR, Lindholm P, Klemi P J, Soderstrom KO,Bergman J, Haaparanta M, Ruotsalainen U, Solin O. Increased glucosemetabolism in untreated non-Hodgkin’s lymphoma: a study with positronemission tomography and flüorine-18-fluorodeoxyglucose. Blood.
  • ;86:3522–3527.
  • Kaida H, Kawahara A, Hayakawa M, Hattori S, Kurata S, Fujimoto K, AzumaK, Hirose Y, Takamori S, Hiromatsu Y, Nakashima T, Fujita H, Kage M,Hayabuchi N, Ishibashi M. The difference in relationship between 18F-FDGuptake and clinicopathological factors on thyroid, esophageal, and lungcancers. Nucl Med Commun. 2014;35:36-43.
  • Vesselle H, Salskov A, Turcotte E, Wiens L, Schmidt R, Jordan CD, VallièresE, Wood DE. Relationship between non-small cell lung cancer FDG uptakeat PET, tumor histology, and Ki-67 proliferation index. J Thorac Oncol.2008;3:971-978.
  • Watanabe K, Nomori H, Ohtsuka T, Naruke T, Ebihara A, Orikasa H, YamazakiK, Uno K, Kobayashi T, Goya T. [F-18]Fluorodeoxyglucose positron emissiontomography can predict pathological tumor stage and proliferative activitydetermined by Ki-67 in clinical stage IA lung adenocarcinomas. Jpn J Clin
  • Oncol. 2006;36:403-409.
  • Zhou M, Sun T, Xing X, Yang J. The Correlation between FDG PET/CT
  • Imaging and Molecule Makers in Non-Small Cell Lung Cancer. Zhongguo
  • Fei Ai Za Zhi. 2009 20;12:172-175.
  • Araz O, Demirci E, Ucar EY, Calik M, Karaman A, Durur-Subasi I, Orsal E,Subasi M, Daloglu F, Akgun M. Roles of Ki-67, p53, transforming growthfactor-
  • Sasaki M, Sugio K, Kuwabara Y, Koga H, Nakagawa M, Chen T, Kaneko K,Hayashi K, Shioyama Y, Sakai S, Honda H. Alterations of tumor suppressorgenes (Rb, p16, p27 and p53) and an increased FDG uptake in lung cancer.Ann Nucl Med. 2003;17:189-96.
  • Duan XY, Wang W, Wang JS, Shang J, Gao JG, Guo YM. Fluorodeoxyglucosepositron emission tomography and chemotherapy-related tumor markerexpression in non-small cell lung cancer. BMC Cancer. 2013;13:546.
  • Nakamura H, Hirata T, Kitamura H, Nishikawa J. Correlation of the
  • standardized uptake value in FDG-PET with the expression level of cellcycle-related molecular biomarkers in resected non-small cell lung cancers.Ann Thorac Cardiovasc Surg. 2009;15:304-10.
  • Tabata K, Tanaka T, Hayashi T, Hori T, Nunomura S, Yonezawa S, FukuokaJ. Ki-67 is a strong prognostic marker of non-small cell lung cancer whentissue heterogeneity is considered. BMC Clin Pathol. 2014;14:23.
  • Takahashi T, Nau MM, Chiba I, Birrer MJ, Rosenberg RK, et al. p53: a
  • frequent target for genetic abnormalities in lung cancer. Science 1989;
  • : 491-494.
  • d'Amato TA, Landreneau RJ, McKenna RJ, Santos RS, Parker RJ. Prevalenceof in vitro extreme chemotherapy resistance in resected nonsmall-cell lungcancer. Ann Thorac Surg. 2006;81:440-446.
  • Thottassery JV, Zambetti GP, Arimori K, Schuetz EG, Schuetz JD. p53-dependent regulation of MDR1 gene expression causes selective resistanceto chemotherapeutic agents. Proc Natl Acad Sci USA. 1997;94:11037-11042.
Yıl 2016, Cilt: 2 Sayı: 3, 0 - 0, 29.09.2016

Öz

Kaynakça

  • Siegel R, Ma J, Zou Z, and Jemal A . Cancer statistics. CA Cancer J Clin.2014;64:9-29.
  • Hillman GG, Lonardo F, Hoogstra DJ, Rakowski J, Yunker CK, Joiner MC,Dyson G, Gadgeel S, Singh-Gupta V. Axitinib Improves Radiotherapy inMurine Xenograft Lung Tumors. Transl Oncol. 2014;7:400-409.
  • Bilir C, Balık MS, Kızılkaya B, Yıldırım S, Gemez S, Bilir F. Serum LactateDehydrogenase Levels May Predict Fentanyl Usage in Patients withMetastatic Cancers for The Treatment of Cancer Related Pain. J hum
  • rhythm. 2016;2(2):78-82.
  • de Geus-Oei L, van Krieken JH, Aliredjo R, Krabbe PF, Frielink C, VerhagenAF, Boerman OC, Oyen WJ. Biological correlates of FDG uptake in nonsmallcell lung cancer. Lung Cancer. 2007; 55: 79–87.
  • Kieninger A, Welsh R, Bendick P, Zelenock G, Chmielewski GW. Positronemissiontomography as a prognostic tool for early-stage lung cancer. AmJ Surg. 2006; 191:433-436.
  • Vesselle H1, Schmidt RA, Pugsley JM, Li M, Kohlmyer SG, Vallires E, WoodDE. Lung cancer proliferation correlates with [F-18]fluorodeoxyglucoseuptake by positron emission tomography. Clin Cancer Res. 2000;6:3837-3844.
  • Higashi K1, Ito K, Hiramatsu Y, Ishikawa T, Sakuma T, Matsunari I, KugaG, Miura K, Higuchi T, Tonami H, Yamamoto I. 18F-FDG uptake by primarytumor as a predictor of intratumoral lymphatic vessel invasion and lymphnode involvement in non-small cell lung cancer: analysis of a multicenterstudy. J Nucl Med. 2005;46:267-273.
  • Zhang ZJ, Chen JH, Meng L, Du JJ, Zhang L, Liu Y, Dai HH. 18F-FDG uptakeas a biologic factor predicting outcome in patients with resected non-smallcelllung cancer. Chin Med J (Engl). 2007;120:125-131.
  • Jeong HJ, Min JJ, Park JM, Chung JK, Kim BT, Jeong JM, Lee DS, Lee
  • MC, Han SK, Shim YS. Determination of the prognostic value of [(18)F]
  • fluorodeoxyglucose uptake by using positron emission tomography in
  • patients with non-small cell lung cancer. 2002;23:865-870.
  • Viberti L, Papotti, M, Abbona G.C, Celano,A, Filosso PL, Bussolati G. Valueof Ki-67 immunostaining in preoperative biopsiesof carcinomas of the lung.Hum. Pathol.1997;28:189-192.
  • Minn H, Joensuu H, Ahonen A, Klemi P. Fluorodeoxyglucose imaging:
  • a method to assess the proliferative activity of human cancer in vivo.
  • Comparison with DNA flow cytometry in head and neck tumors. Cancer
  • (Phila.). 1988;61:1776–1781.
  • Haberkorn U, Strauss LG, Reisser C, Haag D, Dimitrakopoulou A, ZiglerS, Oberdorfer F, Rudat V, VanKaick G. Glucose uptake, perfusion, andcell proliferation in head and neck tumors: relation of positron emissiontomography to flow cytometry. J. Nucl.Med.1991;32: 1548-1555.
  • Lapela M, Leskinen S, Minn HR, Lindholm P, Klemi P J, Soderstrom KO,Bergman J, Haaparanta M, Ruotsalainen U, Solin O. Increased glucosemetabolism in untreated non-Hodgkin’s lymphoma: a study with positronemission tomography and flüorine-18-fluorodeoxyglucose. Blood.
  • ;86:3522–3527.
  • Kaida H, Kawahara A, Hayakawa M, Hattori S, Kurata S, Fujimoto K, AzumaK, Hirose Y, Takamori S, Hiromatsu Y, Nakashima T, Fujita H, Kage M,Hayabuchi N, Ishibashi M. The difference in relationship between 18F-FDGuptake and clinicopathological factors on thyroid, esophageal, and lungcancers. Nucl Med Commun. 2014;35:36-43.
  • Vesselle H, Salskov A, Turcotte E, Wiens L, Schmidt R, Jordan CD, VallièresE, Wood DE. Relationship between non-small cell lung cancer FDG uptakeat PET, tumor histology, and Ki-67 proliferation index. J Thorac Oncol.2008;3:971-978.
  • Watanabe K, Nomori H, Ohtsuka T, Naruke T, Ebihara A, Orikasa H, YamazakiK, Uno K, Kobayashi T, Goya T. [F-18]Fluorodeoxyglucose positron emissiontomography can predict pathological tumor stage and proliferative activitydetermined by Ki-67 in clinical stage IA lung adenocarcinomas. Jpn J Clin
  • Oncol. 2006;36:403-409.
  • Zhou M, Sun T, Xing X, Yang J. The Correlation between FDG PET/CT
  • Imaging and Molecule Makers in Non-Small Cell Lung Cancer. Zhongguo
  • Fei Ai Za Zhi. 2009 20;12:172-175.
  • Araz O, Demirci E, Ucar EY, Calik M, Karaman A, Durur-Subasi I, Orsal E,Subasi M, Daloglu F, Akgun M. Roles of Ki-67, p53, transforming growthfactor-
  • Sasaki M, Sugio K, Kuwabara Y, Koga H, Nakagawa M, Chen T, Kaneko K,Hayashi K, Shioyama Y, Sakai S, Honda H. Alterations of tumor suppressorgenes (Rb, p16, p27 and p53) and an increased FDG uptake in lung cancer.Ann Nucl Med. 2003;17:189-96.
  • Duan XY, Wang W, Wang JS, Shang J, Gao JG, Guo YM. Fluorodeoxyglucosepositron emission tomography and chemotherapy-related tumor markerexpression in non-small cell lung cancer. BMC Cancer. 2013;13:546.
  • Nakamura H, Hirata T, Kitamura H, Nishikawa J. Correlation of the
  • standardized uptake value in FDG-PET with the expression level of cellcycle-related molecular biomarkers in resected non-small cell lung cancers.Ann Thorac Cardiovasc Surg. 2009;15:304-10.
  • Tabata K, Tanaka T, Hayashi T, Hori T, Nunomura S, Yonezawa S, FukuokaJ. Ki-67 is a strong prognostic marker of non-small cell lung cancer whentissue heterogeneity is considered. BMC Clin Pathol. 2014;14:23.
  • Takahashi T, Nau MM, Chiba I, Birrer MJ, Rosenberg RK, et al. p53: a
  • frequent target for genetic abnormalities in lung cancer. Science 1989;
  • : 491-494.
  • d'Amato TA, Landreneau RJ, McKenna RJ, Santos RS, Parker RJ. Prevalenceof in vitro extreme chemotherapy resistance in resected nonsmall-cell lungcancer. Ann Thorac Surg. 2006;81:440-446.
  • Thottassery JV, Zambetti GP, Arimori K, Schuetz EG, Schuetz JD. p53-dependent regulation of MDR1 gene expression causes selective resistanceto chemotherapeutic agents. Proc Natl Acad Sci USA. 1997;94:11037-11042.
Toplam 39 adet kaynakça vardır.

Ayrıntılar

Bölüm Makaleler
Yazarlar

Recep Bedir Bu kişi benim

Baran Yusufoğlu Bu kişi benim

Cemil Bilir Bu kişi benim

Serkan Güngör Bu kişi benim

İbrahim Şehitoğlu Bu kişi benim

Cüneyt Yurdakul Bu kişi benim

Sertaç Asa Bu kişi benim

Hasan Morcalı Bu kişi benim

Yayımlanma Tarihi 29 Eylül 2016
Gönderilme Tarihi 29 Eylül 2016
Yayımlandığı Sayı Yıl 2016 Cilt: 2 Sayı: 3

Kaynak Göster

APA Bedir, R., Yusufoğlu, B., Bilir, C., Güngör, S., vd. (2016). Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study. Journal of Human Rhythm, 2(3).
AMA Bedir R, Yusufoğlu B, Bilir C, Güngör S, Şehitoğlu İ, Yurdakul C, Asa S, Morcalı H. Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study. Journal of Human Rhythm. Eylül 2016;2(3).
Chicago Bedir, Recep, Baran Yusufoğlu, Cemil Bilir, Serkan Güngör, İbrahim Şehitoğlu, Cüneyt Yurdakul, Sertaç Asa, ve Hasan Morcalı. “Relationship Between The 18F-FDG Uptake With Ki-67 and P53 Expression in Patients With Lung Cancer: A Clino-Pathologic Study”. Journal of Human Rhythm 2, sy. 3 (Eylül 2016).
EndNote Bedir R, Yusufoğlu B, Bilir C, Güngör S, Şehitoğlu İ, Yurdakul C, Asa S, Morcalı H (01 Eylül 2016) Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study. Journal of Human Rhythm 2 3
IEEE R. Bedir, B. Yusufoğlu, C. Bilir, S. Güngör, İ. Şehitoğlu, C. Yurdakul, S. Asa, ve H. Morcalı, “Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study”, Journal of Human Rhythm, c. 2, sy. 3, 2016.
ISNAD Bedir, Recep vd. “Relationship Between The 18F-FDG Uptake With Ki-67 and P53 Expression in Patients With Lung Cancer: A Clino-Pathologic Study”. Journal of Human Rhythm 2/3 (Eylül 2016).
JAMA Bedir R, Yusufoğlu B, Bilir C, Güngör S, Şehitoğlu İ, Yurdakul C, Asa S, Morcalı H. Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study. Journal of Human Rhythm. 2016;2.
MLA Bedir, Recep vd. “Relationship Between The 18F-FDG Uptake With Ki-67 and P53 Expression in Patients With Lung Cancer: A Clino-Pathologic Study”. Journal of Human Rhythm, c. 2, sy. 3, 2016.
Vancouver Bedir R, Yusufoğlu B, Bilir C, Güngör S, Şehitoğlu İ, Yurdakul C, Asa S, Morcalı H. Relationship Between The 18F-FDG Uptake with Ki-67 and P53 Expression in Patients with Lung Cancer: A Clino-Pathologic Study. Journal of Human Rhythm. 2016;2(3).