Specific thermographic changes during Walker 256 carcinoma development: differential infrared imaging of tumour, inflammation and haematoma.

BACKGROUND Infrared imaging measures spatial variations in the skin temperature aiming to determine pathological processes; hence possible use of this non-invasive analytical method in cancer detection is emerging. METHODS Infrared thermal imaging was used to detect changes in rat skin surface temperature associated with experimental cancer development (Walker 256 carcinoma), inflammation (upon s.c. Sephadex injection) and haematoma (provoked by s.c. blood coagulate injection). Infrared camera with a geometric resolution of 76,800 pixels, spectral range of 8-14 microm and the minimal detectable temperature resolution of 0.07 degrees C with spatial resolution of 0.48 mm at measuring distance of 30 cm was used to obtain computerised thermal scans. Genuine ThermoWEB software developed for remote internet control as open source software was used. RESULTS The raise of peripheral temperature was observed after induction of local inflammation or haematoma. Opposite to that, transient decrease of the skin surface temperature was observed after tumour transplantation. Progressive growth of tumour was associated with the raise of the skin surface temperature from the 10th day after tumour inoculation, when the tumours developed supportive neoangiogenic blood supply, as verified by histology. CONCLUSION While the raise of peripheral temperature in advanced tumour was caused by neoangiogenesis, the reduction in skin surface temperature in an early period after tumour cell inoculation indicated a decay of transplanted tumour cells due to the immune response and the lack of blood supply. Thus, infrared thermal imaging may have considerable value in evaluation of the tumour development and discrimination of cancer from inflammation and haematoma.

[1]  Y. Miyachi,et al.  Neutrophil chemotaxis, phagocytosis and parameters of reactive oxygen species in human aging: cross-sectional and longitudinal studies. , 1989, Life sciences.

[2]  C. Parish,et al.  Evaluation of the ability of digital infrared imaging to detect vascular changes in experimental animal tumours , 2004, International journal of cancer.

[3]  N. Žarković,et al.  Oxidative burst and anticancer activities of rat neutrophils , 2005, BioFactors.

[4]  D. Hanahan,et al.  Patterns and Emerging Mechanisms of the Angiogenic Switch during Tumorigenesis , 1996, Cell.

[5]  N. Žarković,et al.  The involvement of granulocytes in spontaneous regression of Walker 256 carcinoma. , 2008, Cancer letters.

[6]  N. Žarković,et al.  Oxidative burst of neutrophils against melanoma B16-F10. , 2007, Cancer letters.

[7]  Klein Jh Muscular hematomas: diagnosis and management. , 1990 .

[8]  Rakesh K. Jain,et al.  Normalizing tumor vasculature with anti-angiogenic therapy: A new paradigm for combination therapy , 2001, Nature Medicine.

[9]  Chengli Song,et al.  Thermographic assessment of tumor growth in mouse xenografts , 2007, International journal of cancer.

[10]  Eddie Yin-Kwee Ng,et al.  A Framework for Early Discovery of Breast Tumor Using Thermography with Artificial Neural Network , 2003, The breast journal.

[11]  J. Folkman What is the evidence that tumors are angiogenesis dependent? , 1990, Journal of the National Cancer Institute.

[12]  A. Ballestrero,et al.  Relationship between antibody-dependent tumour cell lysis and primary granule exocytosis by human neutrophils. , 1987, Clinical and experimental immunology.

[13]  A. Ballestrero,et al.  Tumor cell lysis by activated human neutrophils: Analysis of neutrophil-delivered oxidative attack and role of leukocyte function-associated antigen 1 , 1991, Inflammation.

[14]  J. Berek,et al.  Human neutrophil-mediated lysis of ovarian cancer cells. , 1989, Blood.

[15]  K. Skala,et al.  Remote control and measurement of temperature over the web , 2005, 47th International Symposium ELMAR, 2005..

[16]  Rakesh K. Jain,et al.  Pathology: Cancer cells compress intratumour vessels , 2004, Nature.

[17]  A. M. Hicks,et al.  Transferable anticancer innate immunity in spontaneous regression/complete resistance mice , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Hans-Georg Rammensee,et al.  Coordinated Dual Cleavages Induced by the Proteasome Regulator PA28 Lead to Dominant MHC Ligands , 1996, Cell.

[19]  M L KARNOVSKY,et al.  The biochemical basis of phagocytosis. I. Metabolic changes during the ingestion of particles by polymorphonuclear leukocytes. , 1959, The Journal of biological chemistry.

[20]  R. Virchow Die krankhaften Geschwülste : dreissig Vorlesungen, gehalten während des Wintersemesters 1862-1863 an der Universität zu Berlin , 1863 .

[21]  M. Katano,et al.  Neutrophil‐Mediated Tumor Cell Destruction in Cancer Ascites , 1982, Cancer.

[22]  A. Lichtenstein,et al.  Anti‐tumor effect of inelammatory neutrophils: Characteristics of in vivo generation and in vitro tumor cell lysis , 1985, International journal of cancer.

[23]  J. Verhoef,et al.  Uncoupling of Oxidative and Non‐Oxidative Mechanisms in Human Granulocyte‐Mediated Cytotoxicity: Use of Cytoplasts and Cells From Chronic Granulomatous Disease Patient , 1990, Journal of leukocyte biology.

[24]  J. Kalden,et al.  Involvement of the high-affinity receptor for IgG (Fc gamma RI; CD64) in enhanced tumor cell cytotoxicity of neutrophils during granulocyte colony-stimulating factor therapy , 1993 .

[25]  R. Gambari,et al.  Interferon-gamma enhances monoclonal antibody 17-1A-dependent neutrophil cytotoxicity toward colorectal carcinoma cell line SW11-16. , 1994, Clinical immunology and immunopathology.

[26]  F. Patrone,et al.  Antibody-dependent killing of tumor cells by polymorphonuclear leukocytes. Involvement of oxidative and nonoxidative mechanisms. , 1984, Journal of the National Cancer Institute.

[27]  C. Song Effect of local hyperthermia on blood flow and microenvironment: a review. , 1984, Cancer research.