Association between increased tumor necrosis factor alpha levels and acquired activated protein C resistance in patients with metastatic colorectal cancer

被引:18
作者
Ferroni, Patrizia [1 ]
Riondino, Silvia [1 ]
Portarena, Ilaria [2 ]
Formica, Vincenzo [2 ]
La Farina, Francesca [1 ]
Martini, Francesca [1 ]
Massimiani, Gioia [2 ]
Palmirotta, Raffaele [1 ]
Guadagni, Fiorella [1 ]
Roselli, Mario [2 ]
机构
[1] IRCCS San Raffaele Pisana, Dept Lab Med & Adv Biotechnol, I-00163 Rome, Italy
[2] Univ Roma Tor Vergata, Dept Internal Med, Tor Vergata Clin Ctr, Rome, Italy
关键词
Metastatic colorectal cancer; Activated protein C; Tumor necrosis factor alpha; Venous thromboembolism; VENOUS THROMBOEMBOLISM; CARCINOEMBRYONIC ANTIGEN; TNF-ALPHA; INFLAMMATION; THROMBOSIS; CYTOKINES; CHEMOTHERAPY; LEIDEN; BLOOD; RISK;
D O I
10.1007/s00384-012-1493-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose The purpose of this study was to investigate the possible association between tumor necrosis factor-alpha (TNF-alpha) levels and defects in the activated protein C (APC) system as a determinant of venous thromboembolism (VTE) in metastatic colorectal cancer patients (mCRC) undergoing chemotherapy. Methods TNF-alpha levels (measured by immunoassay) and abnormalities in the APC system [evaluated by an APC-dependent thrombin generation assay (ThromboPath-ThP)] were evaluated in 45 mCRC patients undergoing chemotherapy. VTE events were recorded during follow-up. Results TNF-alpha levels were increased (p < 0.01), and APC functionality was decreased (p < 0.0001) in mCRC patients compared to age- and sex-matched controls. An inverse correlation was observed between TNF-alpha and APC impairment in mCRC (p < 0.0001). TNF-alpha was confirmed as an independent predictor (p = 0.007) for APC abnormalities at multivariate regression analysis. Nine (20 %) of 45 mCRC patients experienced VTE during chemotherapy. Bayesian analysis of combined ThP/TNF-alpha showed a positive predictive value of 0.67 in predicting VTE (p = 0.01). Cox proportional hazards survival analysis confirmed the predictive value of combined ThP/TNF-alpha determination in VTE risk assessment of mCRC patients (either negative vs. both positive: HR = 0.02; p = 0.001), and Kaplan-Meier analysis demonstrated that mCRC patients with either negative TNF-alpha or ThP values prior to chemotherapy were less likely to experience VTE (13 %) than patients with abnormalities of both markers (67 %, p = 0.002). Conclusions These results suggest that the host inflammatory response to cancer cells and/or tumor-derived cytokines could be responsible for an impairment of the APC system and a switch toward a pro-thrombotic state, which might predispose to the occurrence of VTE in mCRC patients undergoing chemotherapy.
引用
收藏
页码:1561 / 1567
页数:7
相关论文
共 50 条
  • [21] Association between tumor necrosis factor alpha rs1800629 polymorphism and risk of cervical cancer
    Wan, Lanling
    Ma, Kunpeng
    Wang, Zhiyong
    Mou, Yingying
    Ma, Li
    Guo, Yong
    INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, 2015, 8 (02): : 2108 - 2117
  • [22] Alteration in Serum Levels of Tumor Necrosis Factor Alpha is associated with Histopathologic Progression of Gastric Cancer
    Alikhani, Mehdi
    Esmaeili, Maryam
    Tashakoripour, Mohammad
    Mohagheghi, Mohammad Ali
    Hosseini, Mahmoud Eshagh
    Touati, Eliette
    Vosough, Massoud
    Mohammadi, Marjan
    IRANIAN BIOMEDICAL JOURNAL, 2023, 27 (01) : 72 - 78
  • [23] Association of Single Nucleotide Polymorphisms in Tumor Necrosis Factor-Alpha with Cervical Cancer Susceptibility
    Jin, Ying
    CELL BIOCHEMISTRY AND BIOPHYSICS, 2015, 71 (01) : 77 - 84
  • [24] Correlation between circulating tumor DNA and carcinoembryonic antigen levels in patients with metastatic colorectal cancer
    Osumi, Hiroki
    Shinozaki, Eiji
    Ooki, Akira
    Shimozaki, Keitaro
    Kamiimabeppu, Daisaku
    Nakayama, Izuma
    Wakatsuki, Takeru
    Ogura, Mariko
    Takahari, Daisuke
    Chin, Keisho
    Yamaguchi, Kensei
    CANCER MEDICINE, 2021, 10 (24): : 8820 - 8828
  • [25] Increased expression of tumor necrosis factor-α is associated with advanced colorectal cancer stages
    Al Obeed, Omar A.
    Alkhayal, Khayal A.
    Al Sheikh, Abdulmalik
    Zubaidi, Ahmad M.
    Vaali-Mohammed, Mansoor-Ali
    Boushey, Robin
    Mckerrow, James H.
    Abdulla, Maha-Hamadien
    WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (48) : 18390 - 18396
  • [26] Elevated levels of plasma tumor necrosis factor alpha in patients with pseudoexfoliation glaucoma
    Kondkar, Altaf A.
    Azad, Taif A.
    Almobarak, Faisal A.
    Kalantan, Hatem
    Al-Obeidan, Saleh A.
    Abu-Amero, Khaled K.
    CLINICAL OPHTHALMOLOGY, 2018, 12 : 153 - 159
  • [27] Circulating Leptin, Adiponectin, and Tumor Necrosis Factor-Alpha in Patients Undergoing Surgery Due to Colorectal Cancer
    Tojek, Krzysztof
    Anaszewicz, Marzena
    Szukay, Beata
    Czerniak, Beata
    Socha, Ewa
    Lis, Kinga
    Zbikowska-Gotz, Magdalena
    Bartuzi, Zbigniew
    Banaszkiewicz, Zbigniew
    Budzynski, Jacek
    DIGESTION, 2021, 102 (02) : 246 - 255
  • [28] association of tumor necrosis factor alpha, lymphotoxin alpha, tumor necrosis factor receptor 1 and tumor necrosis factor receptor 2 gene polymorphisms and serum levels with periodontitis and type 2 diabetes in Serbian population
    Petrovic, Sanja Matic
    Nikolic, Nadja
    Toljic, Bosko
    Arambasic-Jovanovic, Jelena
    Milicic, Biljana
    Milicic, Tanja
    Jotic, Aleksandra
    Vidakovic, Melita
    Milasin, Jelena
    Pucar, Ana
    ARCHIVES OF ORAL BIOLOGY, 2020, 120
  • [29] Association between increased C-reactive protein and cardiovascular disease among patients with rectal cancer
    Qiao, Huimin
    Wang, Changxin
    Yang, Chunhong
    Lei, Lei
    Chen, Yijing
    Luo, Yun
    Zeng, Xiangfu
    Guo, You
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [30] Correlation between serum tumor necrosis factor alpha levels and clinical severity of tuberculosis
    de Andrade Junior, Dahia Ramos
    dos Santos, Sania Alves
    de Castro, Isac
    de Andrade, Dahir Ramos
    BRAZILIAN JOURNAL OF INFECTIOUS DISEASES, 2008, 12 (03) : 226 - 233