Survey of risk factors contributed to lymphatic metastasis in patients with oral tongue cancer by immunohistochemistry

被引:43
作者
Zhang, Zhuang [1 ]
Pan, Jian [1 ]
Li, Longjiang [1 ]
Wang, Zhuomin [2 ]
Xiao, Wenlin [3 ]
Li, Ningyi [3 ]
机构
[1] Sichuan Univ, W China Hosp Stomatol, State Key Lab Oral Dis, Chengdu 610041, Peoples R China
[2] PLA 452 Hosp, Chengdu, Peoples R China
[3] Qingdao Univ, Dept Oral & Maxillofacial Surg, Med Sch Hosp, Qingdao 266071, Peoples R China
基金
美国国家科学基金会;
关键词
biomarkers; immunohistochemistry; lymphatic metastasis; oral tongue cancer; risk factor; SQUAMOUS-CELL CARCINOMA; TUMOR LYMPHANGIOGENESIS; NODE METASTASIS; BREAST-CANCER; NECK-CANCER; HEAD; EXPRESSION; FIBRONECTIN; COLLAGEN; GROWTH;
D O I
10.1111/j.1600-0714.2010.00953.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: The aim of this study was to define the biomarkers of lymphatic spread which facilitate the appropriate therapy for oral tongue squamous cell carcinoma (OTSCC) patients at early stage. Here, we investigated the expression levels of seven biomarkers in oral squamous cell carcinoma (OSCC) tissues as well as their associations with the clinicopathologic features of OTSCC patients. Methods: The OTSCC samples were obtained from 138 patients undergoing tumor resection. Immunohistochemical staining was performed by using ColIA, ColIVA, Fn1, MMP-1, MMP-2, uPA, and D2-40 antibodies. Expression level of theses biomarkers in normal and tumor tissues were compared. Risk factors of lymphatic dissemination were evaluated by logistic regression equation. Results: LVD, MMP-1, MMP-2, and uPA in cancer tissues were significantly higher than those in normal tissue, and ColIA, ColIVA, and Fn1 in cancer tissue were significantly lower than those in normal tissue. Similar results were obtained from the comparison between metastatic tumor and non-metastatic tumor. All biomarker expressions were closely related with lymph node status and clinical stage. Additionally, the regression equation demonstrated that LVD is the risk factor of lymphatic metastasis in OTSCC patients (OR = 1.732; 95% CIs: 1.167-2.057; P < 0.05). Conclusions: Down-regulation of ColIA, ColIVA, and Fn1 and up-regulation of LVD, MMP-1, MMP-2, and uPA might be important features of OSCC progression, which may exert their functions and favorably predict lymphatic dissemination for OSCC patients at relatively early stage. Among these biomarkers, increased LVD is an independent risk factor of lymphatic metastasis, which could better predict whether metastasis will occur or not.
引用
收藏
页码:127 / 134
页数:8
相关论文
共 35 条
  • [21] Influence of fast lymphatic drainage on metastatic spread in cutaneous malignant melanoma:: a prospective feasibility study
    Maza, S
    Valencia, R
    Geworski, L
    Sandrock, D
    Zander, A
    Audring, H
    Dräger, E
    Winter, H
    Sterry, W
    Munz, DL
    [J]. EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2003, 30 (04) : 538 - 544
  • [22] Tumor lymphangiogenesis correlates with lymph node metastasis and clinicopathologic parameters in oral squamous cell carcinoma
    Miyahara, Mayumi
    Tanuma, Jun-ichi
    Sugihara, Kazumasa
    Semba, Ichiro
    [J]. CANCER, 2007, 110 (06) : 1287 - 1294
  • [23] Lymphatic metastasis in the absence of functional intratumor lymphatics
    Padera, TP
    Kadambi, A
    di Tomaso, E
    Carreira, CM
    Brown, EB
    Boucher, Y
    Choi, NC
    Mathisen, D
    Wain, J
    Mark, EJ
    Munn, LL
    Jain, RK
    [J]. SCIENCE, 2002, 296 (5574) : 1883 - 1886
  • [24] Clinical significance of MMP-2 and MMP-9 in patients with oral cancer
    Patel, Beena P.
    Shah, Shakuntala V.
    Shukla, Shilin N.
    Shah, Pankaj M.
    Patel, Prabhudas S.
    [J]. HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2007, 29 (06): : 564 - 572
  • [25] Pepper MS, 2001, CLIN CANCER RES, V7, P462
  • [26] Piemonte M, 2003, Acta Otorhinolaryngol Ital, V23, P132
  • [27] Microarray assessment of fibronectin, collagen and integrin expression and the role of fibronectin-collagen coating in the growth of normal, SV40 T-antigen-immortalised and malignant human oral keratinocytes
    Sarang, Z
    Haig, Y
    Hansson, A
    Vondracek, M
    Wärngård, L
    Grafström, RC
    [J]. ATLA-ALTERNATIVES TO LABORATORY ANIMALS, 2003, 31 (06): : 575 - 585
  • [28] Keynote comment: Why the lack of progress for oral cancer?
    Shah, JP
    Singh, B
    [J]. LANCET ONCOLOGY, 2006, 7 (05) : 356 - 357
  • [29] Differential expression of basement membrane collagen-IV αl to α6 chains during oral carcinogenes
    Tamamura, Ryo
    Nagatsuka, Hitoshi
    Siar, Chong Huat
    Katase, Naoki
    Naito, Ichiro
    Sado, Yoshikazu
    Nagai, Noriyuki
    [J]. VIRCHOWS ARCHIV, 2006, 449 (03) : 358 - 366
  • [30] Urtreger AJ, 1999, INT J CANCER, V82, P748, DOI 10.1002/(SICI)1097-0215(19990827)82:5<748::AID-IJC20>3.3.CO