Radiation-induced changes in gene-expression profiles for the SCCVII tumor cells grown in vitro and in vivo

被引:11
作者
Cook, John A.
Chuang, Eric Y.
Tsai, Mong-Hsun
Coffin, Debbie
Degraff, William
Sowers, Anastasia L.
Mitchell, James B.
机构
[1] NCI, Radiat Biol Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[2] Natl Taiwan Univ, Dept Elect Engn, Bioengn Grp, Taipei, Taiwan
关键词
D O I
10.1089/ars.2006.8.1263
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SCCVII tumor cells that grow in vitro or in vivo as a solid tumor were used to compare and contrast gene-expression profiles with or without exposure to two doses of ionizing radiation. Exponentially growing SCCVII cell cultures and tumors (1 cm diameter) were treated with 0, 2, or 10 Gy, and RNA was collected 1, 3, 6, 12, and 24 h after treatment. Growth under in vitro conditions increased the expression of genes associated with the unfolded protein response (UPR) including ATF4, Ero-1 like, and cystathionase. Growth in vivo indicated that the HIF-1a genes were not upregulated, whereas genes such as hemoglobin alpha and crystallin alpha B were significantly upregulated. Ninety genes of 16K were found to be significantly modulated under either growth condition by radiation treatment. Gene expression was not dose dependent. Sixty percent of these genes exhibited similar modulation under both in vitro and in vivo conditions; however, 29% of the genes were modulated by radiation under in vivo conditions only. Gene-expression profiles for the same tumor cells can differ, dependent on growth conditions, underscoring the influence that the tumor microenvironment exerts on gene expression for both growth of solid tumors and their response to radiation treatment.
引用
收藏
页码:1263 / 1272
页数:10
相关论文
共 39 条
[1]  
Amundson SA, 2001, RADIAT RES, V156, P657, DOI 10.1667/0033-7587(2001)156[0657:IOGEAA]2.0.CO
[2]  
2
[3]   p53 inhibits hypoxia-inducible factor-stimulated transcription [J].
Blagosklonny, MV ;
An, WG ;
Romanova, LY ;
Trepel, J ;
Fojo, T ;
Neckers, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :11995-11998
[4]   Inhibition of HIF-1-and wild-type p53-stimulated transcription by codon Arg175 p53 mutants with selective loss of functions [J].
Blagosklonny, MV ;
Giannakakou, P ;
Romanova, LY ;
Ryan, KM ;
Vousden, KH ;
Fojo, T .
CARCINOGENESIS, 2001, 22 (06) :861-867
[5]   Activating transcription factor 4 is translationally regulated by hypoxic stress [J].
Blais, JD ;
Filipenko, V ;
Bi, MX ;
Harding, HP ;
Ron, D ;
Koumenis, C ;
Wouters, BG ;
Bell, JC .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (17) :7469-7482
[6]   A microarray-based, integrated approach to identify novel regulators of cancer drug response and apoptosis [J].
Brachat, A ;
Pierrat, B ;
Xynos, A ;
Brecht, K ;
Simonen, M ;
Brüngger, A ;
Heim, J .
ONCOGENE, 2002, 21 (54) :8361-8371
[7]   Expression and characterization of murine hevin (SC1), a member of the SPARC family of matricellular proteins [J].
Brekken, RA ;
Sullivan, MM ;
Workman, G ;
Bradshaw, AD ;
Carbon, J ;
Siadak, A ;
Murri, C ;
Framson, PE ;
Sage, EH .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2004, 52 (06) :735-748
[8]   Tumor microenvironment and the response to anticancer therapy [J].
Brown, JM .
CANCER BIOLOGY & THERAPY, 2002, 1 (05) :453-458
[9]   Alpha B-crystallin, a new independent marker for poor prognosis in head and neck cancer [J].
Chin, D ;
Boyle, GM ;
Williams, RM ;
Ferguson, K ;
Pandeya, N ;
Pedley, J ;
Campbell, CM ;
Theile, DR ;
Parsons, PG ;
Coman, WB .
LARYNGOSCOPE, 2005, 115 (07) :1239-1242
[10]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868