Identification of the involvement of LOXL4 in generation of keratocystic odontogenic tumors by RNA-Seq analysis

Wei-Peng Jiang , Zi-Han Sima , Hai-Cheng Wang , Jian-Yun Zhang , Li-Sha Sun , Feng Chen , Tie-Jun Li

International Journal of Oral Science ›› 2014, Vol. 6 ›› Issue (1) : 31 -38.

PDF
International Journal of Oral Science ›› 2014, Vol. 6 ›› Issue (1) : 31 -38. DOI: 10.1038/ijos.2013.96
Article

Identification of the involvement of LOXL4 in generation of keratocystic odontogenic tumors by RNA-Seq analysis

Author information +
History +
PDF

Abstract

Gene expression profiling reveals how surrounding tissues may the promote growth of a benign but aggressive class of oral tumor. The process by which keratocystic odontogenic tumors (KCOT) develop is poorly understood, but evidence suggests that KCOT cells receive important cues from the stromal cells that surround the tumor. Researchers led by Tie-Jun Li and Feng Chen of China’s Peking University School and Hospital of Stomatology analyzed and compared the gene activity in KCOT stromal tissue with healthy samples. They identified a secreted protein, LOXL4, which is produced at considerably elevated levels in KCOT samples. Preliminary functional analysis suggests that LOXL4 can stimulate blood vessel growth, and may also promote proliferation and invasive growth in endothelial cells. These findings thus illustrate one possible mechanism by which cells in the tumor environment could stimulate KCOT formation and expansion.

Keywords

angiogenesis / keratocystic odontogenic tumor / lysyl oxidase-like 4 / RNA-sequencing / tumor stromal fibroblast

Cite this article

Download citation ▾
Wei-Peng Jiang, Zi-Han Sima, Hai-Cheng Wang, Jian-Yun Zhang, Li-Sha Sun, Feng Chen, Tie-Jun Li. Identification of the involvement of LOXL4 in generation of keratocystic odontogenic tumors by RNA-Seq analysis. International Journal of Oral Science, 2014, 6(1): 31-38 DOI:10.1038/ijos.2013.96

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Mendes RA, Carvalho JF, van der Waal I. Biological pathways involved in the aggressive behavior of the keratocystic odontogenic tumor and possible implications for molecular oriented treatment—an overview. Oral Oncol, 2010, 46(1): 19-24.

[2]

Figueroa A, Correnti M, Avila M. Keratocystic odontogenic tumor associated with nevoid basal cell carcinoma syndrome: similar behavior to sporadic type. Otolaryngol Head Neck Surg, 2010, 142(2): 179-183.

[3]

Shear MSP. Cysts of the oral and maxillofacial regions, 2007 Oxford

[4]

Pan S, Dong Q, Li TJ. Mechanisms of inactivation of PTCH1 gene in nevoid basal cell carcinoma syndrome: modification of the two-hit hypothesis. Clin Cancer Res, 2010, 16(2): 442-450.

[5]

Browne RM. The pathogenesis of odontogenic cysts: a review. J Oral Pathol, 1975, 4(1): 31-46.

[6]

Bhowmick NA, Moses HL. Tumour stroma interactions. Curr Opin Genet Dev, 2005, 15(1): 97-101.

[7]

Park CC, Bissell MJ, Barcellos-Hoff MH. The influence of the microenvironment on the malignant phenotype. Mol Med Today, 2000, 6(8): 324-329.

[8]

Gadbail AR, Hande A, Chaudhary M. Gondivkar. Tumor angiogenesis in keratocystic odontogenic tumor assessed by using CD-105 antigen. J Oral Pathol Med, 2011, 40(3): 263-269.

[9]

Zhang JY, Dong Q, Li TJ. Differences in collagen fibres in the capsule walls of parakeratinized and orthokeratinized odontogenic cysts. Int J Oral Maxillofac Surg, 2011, 40(11): 1296-1300.

[10]

Vij R, Vij H, Rao NN. Evaluation of collagen in connective tissue walls of odontogenic cysts—a histochemical study. J Oral Pathol Med, 2011, 40(3): 257-262.

[11]

Wang HC, Li TJ. The growth and osteoclastogenic effects of fibroblasts isolated from keratocystic odontogenic tumor. Oral Dis, 2013, 19(2): 162-168.

[12]

Tuch BB, Laborde RR, Xu X. Tumor transcriptome sequencing reveals allelic expression imbalances associated with copy number alterations. PLoS ONE, 2010, 5(2): 9317.

[13]

Mortazavi A, Williams BA, McCue K. Mapping and quantifying mammalian transcriptomes by RNA-Seq. Nat Methods, 2008, 5(7): 621-628.

[14]

Wang ET, Sandberg R, Luo S. Alternative isoform regulation in human tissue transcriptomes. Nature, 2008, 456(7221): 470-476.

[15]

Li H, Handsaker B, Wysoker A. The sequence alignment/map format and SAMtools. Bioinformatics, 2009, 25(16): 2078-2079.

[16]

Levin JZ, Berger MF, Adiconis X. Targeted next-generation sequencing of a cancer transcriptome enhances detection of sequence variants and novel fusion transcripts. Genome Biol, 2009, 10(10): R115.1-R115.8.

[17]

Wang Z, Gerstein M, Snyder M. RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet, 2009, 10(1): 57-63.

[18]

Weise JB, Csiszar K, Gottschlich S. Vaccination strategy to target lysyl oxidase-like 4 in dendritic cell based immunotherapy for head and neck cancer. Int J Oncol, 2008, 32(2): 317-322.

[19]

Weise JB, Csiszar K, Gottschlich S. LOXL4 is a selectively expressed candidate diagnostic antigen in head and neck cancer. Int J Oncol, 2008, 44(9): 1323-1331.

[20]

Jaeger TM, Weidner N, Chew K. Tumor angiogenesis correlates with lymph node metastases in invasive bladder cancer. J Urol, 1995, 154(1): 69-71.

[21]

Wallerman O, Motallebipour M, Enroth S. Molecular interactions between HNF4a, FOXA2 and GABP identified at regulatory DNA elements through ChIP-sequencing. Nucleic Acids Res, 2009, 37(22): 7498-7508.

[22]

Shih YH, Chang KW, Chen MY. Lysyl oxidase and enhancement of cell proliferation and angiogenesis in oral squamous cell carcinoma. Head Neck, 2012, 35(2): 250-256.

[23]

Bignon M, Pichol-Thievend C, Hardouin J. Lysyl oxidase-like protein-2 regulates sprouting angiogenesis and type IV collagen assembly in the endothelial basement membrane. Blood, 2011, 118(14): 3979-3989.

[24]

Philipsen HP Om keratocystedr (kolesteratomer) i and kaeberne. Tandlaegebladet, 1956, 60: 963-971.

[25]

Jurisic M, Andric M, dos Santos JN. Clinical, diagnostic and therapeutic features of keratocystic odontogenic tumors: a review. J BUON, 2012, 17(2): 237-244.

[26]

Barnes L, Eveson J, Reichart P. World Health Organization classification of tumours: pathology and genetics of head and neck tumours. Ear Nose Throat J, 2006, 85(2): 74.

[27]

Tsuneki M, Cheng J, Maruyama S. Perlecan-rich epithelial linings as a background of proliferative potentials of keratocystic odontogenic tumor. J Oral Pathol Med, 2008, 37(5): 287-293.

[28]

Pan S, Li TJ. PTCH1 mutations in odontogenic keratocysts: are they related to epithelial cell proliferation. Oral Oncol, 2009, 45(10): 861-865.

[29]

Mendes RA, Carvalho JF, van der Waal I. A comparative immunohistochemical analysis of COX-2, p53, and Ki-67 expression in keratocystic odontogenic tumors. Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 2011, 111(3): 333-339.

[30]

Hirshberg A, Sherman S, Buchner A. Collagen fibres in the wall of odontogenic keratocysts: a study with picrosirius red polarization microscopy. J Oral Pathol Med, 1999, 28(9): 410-412.

[31]

Shear M. The aggressive nature of the odontogenic keratocyst: is it a benign cystic neoplasm? Part 3. Immunocytochemistry of cytokeratin and other epithelial cell markers. Oral Oncol, 2002, 38(5): 407-415.

[32]

Scola N, Gorogh T. LOXL4 as a selective molecular marker in primary and metastatic head/neck carcinoma. Anticancer Res, 2010, 30(11): 4567-4571.

[33]

el-Labban NG, Aghabeigi B. A comparative stereologic and ultrastructural study of blood vessels in odontogenic keratocysts and dentigerous cysts. J Oral Pathol Med, 1990, 19(10): 442-446.

[34]

Alaeddini M, Salah S, Dehghan F. Comparison of angiogenesis in keratocystic odontogenic tumours, dentigerous cysts and ameloblastomas. Oral Dis, 2009, 15(6): 422-427.

[35]

Kotake S, Nanke Y, Kawamoto M. T-cell leukemia translocation-associated gene (TCTA) protein is required for human osteoclastogenesis. Bone, 2009, 45(4): 627-639.

[36]

Manojlovic Z, Stefanovic. A novel role of RNA helicase A in regulation of translation of type I collagen mRNAs. RNA, 2012, 18(2): 321-324.

[37]

Challa AA, Stefanovic B. A novel role of vimentin filaments: binding and stabilization of collagen mRNAs. Mol Cell Biol, 2011, 31(18): 3773-3789.

[38]

Wang J, Lippman SM, Lee JJ. Genetic variations in regulator of G-protein signaling genes as susceptibility loci for second primary tumor/recurrence in head and neck squamous cell carcinom. Carcinogenesis, 2010, 31(10): 1755-1761.

[39]

Manzur M, Hamzah J, Ganss R. Modulation of G protein signaling normalizes tumor vessels. Cancer Res, 2009, 69(2): 396-399.

[40]

Yang S, Li YP. RGS12 is essential for RANKL-evoked signaling for terminal differentiation of osteoclasts in vitro. J Bone Miner Res, 2007, 22(1): 45-54.

AI Summary AI Mindmap
PDF

158

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/