Please wait a minute...
Frontiers in Biology

ISSN 1674-7984

ISSN 1674-7992(Online)

CN 11-5892/Q

Front Biol Chin    2009, Vol. 4 Issue (1) : 82-88    https://doi.org/10.1007/s11515-008-0075-1
Research Article
Analysis of genotype polymorphism of tumor-related genes harbored in chromosome arm 1p and 8p in hepatocellular carcinoma patients by cSNP chip
Juan WANG1(), Wenqin SONG2
1. College of Life Sciences, Shenzhen University; 2. College of Life Sciences, Nankai University
 Download: PDF(182 KB)   HTML
 Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks
Abstract

The majority of single nucleotide polymorphisms (SNPs) found in the coding region (cSNPs) are single base substitutions that may or may not lead to amino acid substitutions, most of which are related to diseases. Some cSNPs may prove useful for their potential links to functional cSNPs via linkage disequilibrium mapping. We have selected 48 cSNPs located in the coding regions of 25 genes to construct the cSNP chip. These genes are harbored in the high frequency loss regions of the chromosome 1p and 8p and related with apoptosis, cell cycles, signal transduction, oncogene, tumor suppressor genes and so on. All of the cSNPs can lead to amino acid substitutions except TP73 (rs1801174). The PCR products amplified from 31 hepatocellular carcinoma (HCC) specimens were labeled with Dig-dUTP and then hybridized with the cSNP chips. The results showed that there was no hybridization signal when there was more than one site of mutation in the amplification sequence, indicating that the cSNP chip had a high sensitivity. The statistic data of the SNP (MT, homozygous and HT, heterozygous) in the HCC patients with different phenotypes (HBV +/-,differentiation stage, family history positive or negative, tumor size) indicated that the number of MT was distinctly different between patients with positive HBV and negative HBV. The MT and HT numbers of all the 48 cSNPs were significantly different between low differentiation and high differentiation HCC patients. The numbers of MT and HT were not different between positived and negative family history groups and between tumor size > 3 cm and ≤ 3 cm groups. The study results provided useful information for understanding the molecular mechanisms of HCC development.

Keywords polymorphism      hepatocellular carcinoma      single nucleotide polymorphisms (SNPs) in coding region (cSNPs)      tumor-related genes      1p and 8p     
Corresponding Author(s): WANG Juan,Email:wangjuan@szu.edu.cn   
Issue Date: 05 March 2009
 Cite this article:   
Juan WANG,Wenqin SONG. Analysis of genotype polymorphism of tumor-related genes harbored in chromosome arm 1p and 8p in hepatocellular carcinoma patients by cSNP chip[J]. Front Biol Chin, 2009, 4(1): 82-88.
 URL:  
https://academic.hep.com.cn/fib/EN/10.1007/s11515-008-0075-1
https://academic.hep.com.cn/fib/EN/Y2009/V4/I1/82
No.genderage/yrHBV infectionHCV infectionfamily history of cancertumor size/cmdifferentiation degreeother information
1male67-++11.0 × 9.0 × 6.0high
2male64---2.0 × 2.0 × 2.0high
3male37---2.5 × 2.0 × 2.0low
4female59---5.5 × 4.0 × 3.0lowdiffuse type
5female48+--7.5 × 8.0 × 7.0highwith clear margin
6male64++-9.5 × 6.2 × 3.5low
7male70+--3.0 × 1.5 × 1.0Lowmultifocal, diffuse type
8male62+--5.5 × 5.5 × 6.0highwith clear margin
9female57+--3.5 × 5.5 × 3.0high
10male52+--6.0 × 4.0 × 3.0highmultifocal
11female40---3.0 × 2.0 × 2.0high
12male56+--7.0 × 6.0 × 3.5highwith clear margin
13male50+--13.0 × 8.0 × 6.0low
14female67---9.0 × 5.0 × 7.0low
15male46--+12.0 × 11.0 × 6.0low
16male45+--9.0 × 9.5 × 5.0lowmultifocal
17male55+--6.0 × 3.5 × 3.0low
18male61++-5.0 × 5.0 × 6.0low
19male57+-+8.0 × 6.0 × 3.5high
20male44+--6.0 × 4.5 × 3.5low
21female55+--5.0 × 4.0 × 3.5highwith clear margin
22female60---3.0 × 4.0 × 3.0high
23male66+--9.0 × 5.5 × 3.0high
24male49---7.0 × 5.2 × 4.0low
25female58-+-11.0 × 8.5 × 5.0lowdiffuse type
26male52+--3.0 × 2.5 × 1.0high
27male65+--6.0 × 4.5 × 3.0high
28male35+--no recordno record
29male40+--no recordno record
30male57+--no recordno record
31male42+--no recordno record
Tab0  Data of the HCC patients
Fig0  Results of touch-down and multiple-primer PCR amplification. M: 100 bp marker (from 100 to 600 bp); lanes 1–15: multi-primer PCR products
1 CargillM, AltshulerD, IrelandJ, SklarP, ArdlieK, PatilN, ShawN, LaneC R, LimE P, KalyanaramanN, NemeshJ, ZiaugraL, FriedlandL, RolfeA, WarringtonJ, LipshutzR, DaleyG Q, LanderE S (1999). Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nature Genetics , 22(3): 231–238
doi: 10.1038/10290
2 ChanK L, LeeJ M F, GuanX Y, FanS T, NgI O L (2002). High-density allelotyping of chromosome 8p in hepatocellular carcinoma and clinicopathologic correlation. Cancer , 94(12): 3179–3185
doi: 10.1002/cncr.10612
3 DeB K, SrinivasanA (1989). Multiple primer pairs for the detection of HTLV-I by PCR. Nucleic Acids Research , 17(5): 2142.
doi: 10.1093/nar/17.5.2142
4 DurigonE L, ErdmanD D, GaryG W, PallanschM A, TorokT J, AndersonL J (1993). Multiple primer pairs for polymerase chain reaction (PCR) amplification of human parvovirus B19 DNA. J Virol Methods , 44(2–3): 155–165
doi: 10.1016/0166-0934(93)90051-R
5 FarrandK, DelahuntB, WangX L, McIverB, HayI D, GoellnerJ R, EberhardtN L, GrebeS K (2002). High resolution loss of heterozygosity mapping of 17p13 in thyroid cancer: Hurthle cell carcinomas exhibit a small 411-kilobase common region of allelic imbalance, probably containing a novel tumor suppressor gene. Journal of Clinical Endocrinology and Metabolism , 87(10): 4715–4721
doi: 10.1210/jc.2002-020708
6 GaoY T, ChenR Y, SongW Q, ChenC B, QiZ L, JingL, SunJ Y, QianS C (2003). DNA microarray for monitoring genetic variability of hepatitis B virus during lamivudine therapy. Chinese Journal of Virologica Sinica , 18: 523–529 (in Chinese)
7 HuberM, MundleinA, DornstauderE, SchneebergerC, TempferC B, MuellerM W, SchmidtW M (2002). Accessing single nucleotide polymorphisms in genomic DNA by direct multiplex polymerase chain reaction amplification on oligonucleotide microarrays. Analytical Biochemistry , 303(1): 25–33
doi: 10.1006/abio.2001.5565
8 IwamotoK, BundoM, UedaJ, NakanoY, UkaiW, HashimotoE, SaitoT, KatoT (2007). Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow. Public of Library of Science , 2(12): e1306
9 LiS P, WangH Y, LiJ Q, ZhangC Q, FengQ S, HuangP, YuX J, HuangL X, LiangQ W, ZengY X (2001). Genome-wide analyses on loss of heterozygosity in hepatocellular carcinoma in Southern China. Journal of Hepatology , 34(6): 840–849
doi: 10.1016/S0168-8278(01)00047-2
10 LuT, HanoH, MengC, NagatsumaK, ChibaS, IkegamiM (2007). Frequent loss of heterozygosity in two distinct regions, 8p23.1 and 8p22, in hepatocellular carcinoma. World Journal of Gastroenterology , 13(7): 1090–1097
11 MidorikawaY, YamamotoS, IshikawaS, KamimuraN, IgarashiH, SugimuraH, MakuuchiM, AburataniH (2006). Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays. Oncogene , 25(40): 5581–5590
doi: 10.1038/sj.onc.1209537
12 MonzonF A, HagenkordJ M, Lyons-WeilerM A, BalaniJ P, ParwaniA V, SciulliC M, LiJ, ChandranU R, BastackyS I, DhirR (2008). Whole genome SNP arrays as a potential diagnostic tool for the detection of characteristic chromosomal aberrations in renal epithelial tumors. Modern Pathology , Feb 8 [Epub ahead of print]
13 NiuJ Y, ShenH B (2000). Application and purification of DNA from clotted blood. Journal of Nanjing Medical University , 20(5): 389–340 (in Chinese)
14 PandyaG A, HolmesM H, SunkaraS, SparksA, BaiY, VerrattiK, SaeedK, VenepallyP, JarrahiB, FleischmannR D, PetersonS N (2007). A bioinformatic filter for improved base-call accuracy and polymorphism detection using the Affymetrix GeneChip whole-genome resequencing platform. Nucleic Acids Research , 35(21): e148
doi: 10.1093/nar/gkm918
15 SambrookJ, RussellD W (2003). Molecular Cloning: A Laboratory Manual, 3rd ed. Huang P T translation. Beijing: Science Press, 483–485 (in Chinese)
16 ShaoJ, LiH, LiewC T, WuQ, LiangX, HouJ (1999). A preliminary study of loss of heterozygosity on chromosome 1p in primary hepatocellular carcinoma, Chinese Journal of Pathology , 28(1): 28–30 (in Chinese)
17 TamuraG (2006). Alterations of tumor suppressor and tumor-related genes in the development and progression of gastric cancer. World Journal of Gastroenterology , 12(2): 192–198
18 WangD G, FanJ B, SiaoC J, BernoA, YoungP, SapolskyR, GhandourG, PerkinsN, WinchesterE, SpencerJ, KruglyakL, SteinL, HsieL, TopaloglouT, HubbellE, RobinsonE, MittmannM, MorrisM S, ShenN, KilburnD, RiouxJ, NusbaumC, RozenS, HudsonT J, LipshutzR, CheeM, LanderE S (1998). Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science , 280: 1077–1082
doi: 10.1126/science.280.5366.1077
19 WangJ, NiH, ChenL, LiuY X, ChenC B, SongW Q (2005). Preparation and analysis of cSNP chip on hepatocellular carcinoma-related genes. Hepatobiliary & Pancreatic Diseases International , 4: 398–402
20 ZhuG N, ZuoL, ZhouQ, ZhangS M, ZhuH Q, GuiS Y, WangY (2004). Loss of heterozygosity on chromosome 10q22-10q23 and 22q11.2-22q12.1 and p53 gene in primary hepatocellular carcinoma. World Journal of Gastroenterology , 10(13): 1975–1978
[1] Narjes Feizollahi, Zeinab Deris Zayeri, Najme Moradi, Mahvash Zargar, Hadi Rezaeeyan. The effect of coagulation factors polymorphisms on abortion[J]. Front. Biol., 2018, 13(3): 190-196.
[2] Habib Haybar, Zeinab Deris Zayeri. The value of using polymorphisms in anti-platelet therapy[J]. Front. Biol., 2017, 12(5): 349-356.
[3] Karim Mowla, Mohammad Amin Saki, Mohammad Taha Jalali, Zeinab Deris Zayeri. How to manage rheumatoid arthritis according to classic biomarkers and polymorphisms?[J]. Front. Biol., 2017, 12(3): 183-191.
[4] Seyed Mehdi Sajjadi,Abbas Khosravi,Jalil Pakravesh,Zahra-soheila Soheili,Shahram Samiei,Saeed Mohammadi,Mohammad Ali Jalali far. Factor XIII Val34Leu polymorphism and risk of recurrent pregnancy loss in Iranian population: a case control study[J]. Front. Biol., 2016, 11(6): 471-475.
[5] Kazuhiro TANAKA, Nikhat J. SIDDIQI, Abdullah S. ALHOMIDA, Akhlaq A. FAROOQUI, Wei-Yi ONG. Differential regulation of cPLA2 and iPLA2 expression in the brain[J]. Front Biol, 2012, 7(6): 514-521.
[6] Yingqing LU. Functional significance of genetic polymorphisms[J]. Front Biol Chin, 2009, 4(3): 266-270.
[7] ZHANG Yong, CHEN Yuqing, TANG Yingchun, ZHANG Kouxing. Combination of ARDRA and RAPD genotyping techniques in identification of spp. genomic species[J]. Front. Biol., 2008, 3(4): 397-401.
[8] LUO Yi, WANG Xujie, MEI Mantong, ZHUANG Chuxiong, ZHOU Feng, YAO Juan, ZHAO Junliang, WEI Zengquan, XIE Hongmei. Genomic polymorphism in consecutive generation rice plants from seeds on board a spaceship and their relationship with space HZE particles[J]. Front. Biol., 2007, 2(3): 297-302.
[9] WANG Juan, NI Hong, CHEN Li, CHEN Chengbin, SONG Wenqin. Polymorphism attribution of cSNPs in cancer-related genes located in loss regions with a high frequency of HCC between HBV and health groups[J]. Front. Biol., 2007, 2(3): 272-275.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed