Flow cytometric analysis of DNA content in parotid tumor and its contiguous acini

被引:0
|
作者
Shengrong Z. [1 ]
Xiuli W. [2 ]
Lenan S. [1 ]
Weimin C. [1 ]
Xinming C. [2 ]
Huihua W. [1 ]
机构
[1] Center of Stomatological Medicine, Tongji Hospital, Tongji Medical University, Wuhan
[2] College of Stomatology, Hubei Medical University, Wuhan
关键词
parotid tumors; contiguous acini; flow cytometry; DNA;
D O I
10.1007/BF02887687
中图分类号
学科分类号
摘要
To investigate the relationship between proliferative capacity of salivary gland cells in contiguous acini of parotid tumors and recurrent neoplasma, DNA contents of 30 fresh specimens of parotid were studied by using cytometry in tumors, normal and shallow or deep lobe acini of the masses. The results showed that the DI was 1.369, S% 16.95, PI 26.18 in malignant tumors; DI was 1.171, S% 12.41, PI 15.54 in recurrent pleomorphic adenoma; DI was 1.141, S% 12. 74, PI 13.07 in pleomorphic adenoma, DI was 0.999, S% 5.10, PI 8.00 in normal acini. Analysis of variance showed there was a significant difference (P < 0.01). The average DNA contents of shallow on deep lobe of contiguous tumors was 1.08 in DI, 10.65 in S%, 13.49 in PI in malignant tumor, 1.06 in DI, 8.96 in S% and 9.85 in PI in pleomorphic adenoma, which were all higher than in normal acini (P > 0.05). It was concluded that the levels of DI and S% of parotid tumor and its contiguous acini are related to degree of malignancy or recurrent condition of the tumors, suggesting contiguous acini of parotid tumors had the strong capacity of proliferation, which might play an important role in recurrent or malignant change of the parotid tumors.
引用
收藏
页码:86 / 88
页数:2
相关论文
共 50 条
  • [21] Flow cytometric analysis of the DNA content of bovine and human bone marrow cells
    Hoeben, D
    Burvenich, C
    Lenjou, M
    Nijs, G
    Massart-Leën, AM
    Van Bockstaele, D
    VETERINARY QUARTERLY, 2000, 22 (02) : 117 - 120
  • [22] DNA CONTENT AND CELL-KINETICS IN COLORECTAL-CARCINOMA - FLOW CYTOMETRIC ANALYSIS OF PRIMARY TUMOR AND LIVER METASTASES
    DANOVA, M
    DERENZIS, MR
    GIRINO, M
    VALENTI, L
    MORA, O
    SCABINI, M
    MAZZINI, G
    RICCARDI, A
    TUMORI, 1995, 81 (03) : 12 - 15
  • [23] Flow cytometric analysis of DNA content for four commercially important crabs in China
    LIU Lei
    CUI Zhaoxia
    SONG Chengwen
    LIU Yuan
    HUI Min
    WANG Chunlin
    ActaOceanologicaSinica, 2016, 35 (06) : 7 - 11
  • [24] The diagnostic value of flow cytometric analysis of DNA content heterogeneity for breast carcinomas
    He, LX
    Mao, YR
    Zhou, JL
    Yang, F
    Zhang, GM
    Feng, ZH
    PHOTONICS AND IMAGING IN BIOLOGY AND MEDICINE, 2003, 5254 : 393 - 398
  • [25] Flow cytometric analysis of DNA content for four commercially important crabs in China
    Lei Liu
    Zhaoxia Cui
    Chengwen Song
    Yuan Liu
    Min Hui
    Chunlin Wang
    Acta Oceanologica Sinica, 2016, 35 : 7 - 11
  • [26] FLOW CYTOMETRIC DNA ANALYSIS OF THYROID-CARCINOMA
    TSUCHIYA, A
    SEKIKAWA, K
    ANDO, Y
    SUZUKI, S
    KIMIJIMA, I
    ABE, R
    JAPANESE JOURNAL OF SURGERY, 1990, 20 (05): : 510 - 514
  • [27] DNA FLOW CYTOMETRIC ANALYSIS OF HEMANGIOPERICYTOMA
    FINN, WG
    GOOLSBY, CL
    SAMBASIVA, M
    AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1994, 101 (02) : 181 - 185
  • [28] Application of the crypt isolation technique to the flow cytometric analysis of DNA content in gastric carcinoma
    Jiao, YF
    Sugai, T
    Suzuki, M
    Uesugi, N
    Habano, W
    Nakamura, SI
    Takagane, A
    Suto, T
    Yoshida, T
    HUMAN PATHOLOGY, 2004, 35 (05) : 587 - 593
  • [29] FLOW CYTOMETRIC ANALYSIS OF DNA CONTENT IN FOCAL NODULAR HYPERPLASIA AND HEPATOCELLULAR-CARCINOMA
    KOPPER, L
    LAPIS, K
    SCHAFF, Z
    MIHALIK, R
    KARACSONY, S
    SZECSENY, A
    NEOPLASMA, 1991, 38 (03) : 257 - 263
  • [30] FLOW CYTOMETRIC ANALYSIS OF DNA CONTENT AND CELL-KINETICS IN COLORECTAL-CARCINOMA
    DAGNANO, I
    COSIMELLI, M
    LAPERA, A
    CAVALIERE, F
    MANNELLA, E
    GIANNARELLI, D
    CAVALIERE, R
    ZUPI, G
    ANTICANCER RESEARCH, 1993, 13 (03) : 699 - 704