Single domain antibody against carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) inhibits proliferation, migration, invasion and angiogenesis of pancreatic cancer cells

被引:24
|
作者
Cheng, Tsai-Mu [1 ,2 ]
Murad, Yanal M. [2 ]
Chang, Chia-Ching [1 ,3 ]
Yang, Ming-Chi [4 ]
Baral, Toya Nath [2 ]
Cowan, Aaron [2 ]
Tseng, Shin-Hua [1 ]
Wong, Andrew [2 ]
MacKenzie, Roger [2 ]
Shieh, Dar-Bin [5 ]
Zhang, Jianbing [2 ]
机构
[1] Natl Chiao Tung Univ, Dept Biol Sci & Technol, Hsinchu 30050, Taiwan
[2] Natl Res Council Canada, Inst Biol Sci, Ottawa, ON K1A 0R6, Canada
[3] Acad Sinica, Inst Phys, Taipei 10529, Taiwan
[4] Natl Synchrotron Radiat Res Ctr, Life Sci Grp, Sci Res Div, Hsinchu, Taiwan
[5] Natl Cheng Kung Univ, Coll Med & Hosp, Inst Oral Med, Tainan 70101, Taiwan
关键词
CEACAM6; Single domain antibodies; Pancreatic cancer; Gemcitabine; Angiogenesis; MMP-9; BxPC3; HEAVY-CHAIN ANTIBODIES; ADENOCARCINOMA CELLS; EXPRESSION PATTERNS; THERAPY; CARCINOMA; TARGET; MICROENVIRONMENT; RESISTANCE; PROMOTES; SURVIVAL;
D O I
10.1016/j.ejca.2012.07.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) is over-expressed in pancreatic cancer cells, and it is associated with the progression of pancreatic cancer. We tested a single domain antibody (sdAb) targeting CEACAM6, 2A3, which was isolated previously from a llama immune library, and an Fc conjugated version of this sdAb, to determine how they affect the pancreatic cancer cell line BxPC3. We also compared the effects of the antibodies to gemcitabine. Gemcitabine and 2A3 slowed down cancer cell proliferation. However, only 2A3 retarded cancer cell invasion, angiogenesis within the cancer mass and BxPC3 cell MMP-9 activity, three features important for tumour growth and metas- tasis. The IC(50)s for 2A3, 2A3-Fc and gemcitabine were determined as 6.5 mu M, 8 mu M and 12 nM, respectively. While the 2A3 antibody inhibited MMP-9 activity by 33% compared to non-treated control cells, gemcitabine failed to inhibit MMP-9 activity. Moreover, 2A3 and 2A3-Fc inhibited invasion of BxPC3 by 73% compared to non-treated cells. When conditioned media that were produced using 2A3- or 2A3-Fc-treated BxPC3 cells were used in a capillary formation assay, the capillary length was reduced by 21% and 49%, respectively. Therefore 2A3 is an ideal candidate for treating tumours that over-express CEACAM6. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:713 / 721
页数:9
相关论文
共 50 条
  • [1] Carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) is a potential biomarker for peritoneal metastasis of gastric cancer
    Lung, Lydia K.
    Hui, Angela M.
    Leung, Billy C.
    Chen, George G.
    Ng, Enders K.
    [J]. GASTROENTEROLOGY, 2008, 134 (04) : A306 - A306
  • [2] The Role of Biliary Carcinoembryonic Antigen-Related Cellular Adhesion Molecule 6 (CEACAM6) as a Biomarker in Cholangiocarcinoma
    Rose, J. Bart
    Correa-Gallego, Camilo
    Li, Yu
    Nelson, James
    Alseidi, Adnan
    Helton, W. Scott
    Allen, Peter J.
    D'Angelica, Michael I.
    DeMatteo, Ronald P.
    Fong, Yuman
    Kingham, T. Peter
    Kowdley, Kris V.
    Jarnagin, William R.
    Rocha, Flavio G.
    [J]. PLOS ONE, 2016, 11 (03):
  • [3] Carcinoembryonic antigen-related Cell Adhesion Molecule 6 (CEACAM6) promotes the Development of Lung Metastases in advanced Prostate Carcinomas
    Saraji, A.
    Hempel, K.
    Stegmann-Frehse, J.
    Duan, K.
    Offermann, A.
    Krupar, R.
    Watermann, C.
    Jonigk, D.
    Kuehnel, M. P.
    Kirfel, J.
    Perner, S.
    Sailer, V
    [J]. ONCOLOGY RESEARCH AND TREATMENT, 2022, 45 (SUPPL 2) : 187 - 187
  • [4] Carcinoembryonic Antigen-Related Cell Adhesion Molecules (CEACAM) 1, 5 and 6 as Biomarkers in Pancreatic Cancer
    Gebauer, Florian
    Wicklein, Daniel
    Horst, Jennifer
    Sundermann, Philipp
    Maar, Hanna
    Streichert, Thomas
    Tachezy, Michael
    Izbicki, Jakob R.
    Bockhorn, Maximilian
    Schumacher, Udo
    [J]. PLOS ONE, 2014, 9 (11):
  • [5] Influenza A Virus Neuraminidase Protein Enhances Cell Survival through Interaction with Carcinoembryonic Antigen-related Cell Adhesion Molecule 6 (CEACAM6) Protein
    Gaur, Pratibha
    Ranjan, Priya
    Sharma, Shipra
    Patel, Jenish R.
    Bowzard, J. Bradford
    Rahman, Shah K.
    Kumari, Rashmi
    Gangappa, Shivaprakash
    Katz, Jacqueline M.
    Cox, Nancy J.
    Lal, Renu B.
    Sambhara, Suryaprakash
    Lal, Sunil K.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (18) : 15109 - 15117
  • [6] High Expression of Carcinoembryonic Antigen-Related Cell Adhesion Molecule(CEACAM) 6 In Primary Myelofibrosis
    Hasselbalch, Hans Carl
    Skov, Vibe
    Larsen, Thomas Stauffer
    Thomassen, Mads
    Riley, Caroline
    Jensen, Morten Krogh
    Bjerrum, Ole Weis
    Kruse, Torben A.
    [J]. BLOOD, 2010, 116 (21) : 1675 - 1676
  • [7] CEACAM6 (CELL ADHESION MOLECULE 6 RELATED TO CARCINOEMBRYONIC ANTIGEN): A POSSIBLE ROLE IN PEDIATRIC CROHN'S DISEASE?
    Costanzo, M.
    Pierdomenico, M.
    Stronati, L.
    Negroni, A.
    Vitali, R.
    Di Camillo, C.
    Del Giudice, E.
    Cavallari, N.
    Cucchiara, S.
    [J]. JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2010, 50 : E99 - E100
  • [8] High expression of carcinoembryonic antigen-related cell adhesion molecule (CEACAM) 6 and 8 in primary myelofibrosis
    Hasselbalch, Hans Carl
    Skov, Vibe
    Larsen, Thomas Stauffer
    Thomassen, Mads
    Riley, Caroline Hasselbalch
    Jensen, Morten K.
    Bjerrum, Ole Weis
    Kruse, Torben A.
    [J]. LEUKEMIA RESEARCH, 2011, 35 (10) : 1330 - 1334
  • [9] RNA interference targeting carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM-6): a novel strategy for the treatment of pancreatic adenocarcinoma
    Duxbury, MS
    Matros, E
    Redston, M
    Ashley, SW
    Whang, EE
    [J]. BRITISH JOURNAL OF SURGERY, 2004, 91 (09) : 1213 - 1213
  • [10] The expression of carcinoembryonic antigen-related cell adhesion molecule 6 and 8 in breast cancer
    Iwabuchi, Erina
    Miki, Yasuhiro
    Takagi, Kiyoshi
    Onodera, Yoshiaki
    Shibahara, Yukiko
    Ishida, Takanori
    Suzuki, Takashi
    Sasano, Hironobu
    [J]. CANCER RESEARCH, 2019, 79 (13)