Skip to main content

Metallothionein expression in feline injection site fibrosarcomas

Abstract

Background

Feline injection site fibrosarcoma is an aggressive and infiltrative tumour arising in the background of chronic inflammation. The aim of this study was to evaluate the expression of metallothionein (I-II) in feline injection site fibrosarcomas and to assess its possible relationships with Ki67 index, inflammation score and tumour grade. The study included 40 feline fibrosarcomas, located in the common injection sites (i.e., interscapular area, thigh, flank), constituting archival diagnostic specimens collected between 2019–2020. Tumours were graded histologically according to the newly proposed soft-tissue sarcoma grading system in cats. Immunohistochemistry was performed to evaluate the expression of Ki67 and metallothionein in tumour cells.

Results

The cytoplasmic and sometimes nuclear expression of metallothionein was observed in all tumours grade I, 66.67% of tumours grade II and 55% of tumours grade III. The expression of metallothionein was negatively correlated with tumour grade and inflammation score, while the Ki67 index was positively correlated with tumour grade, inflammation score and necrosis score.

Conclusion

The downregulation of MT expression in feline injection site fibrosarcomas seems to be connected with an increase in the inflammatory infiltration, hence tumour progression. This is the first study describing metallothionein expression in feline injection site fibrosarcomas.

Peer Review reports

Background

Feline injection site sarcoma (FISS) is a malignant tumour arising in the area of a former injection site [1, 2]. The vast majority of FISSs are fibrosarcomas, however other malignancies such as osteosarcoma, chondrosarcoma, rhabdomyosarcoma, malignant fibrous histiocytoma and myofibroblastic sarcoma have also been reported [3]. Although the first cases of FISS in cats were related to the increased use of rabies and feline leukaemia virus (FeLV) vaccinations [4,5,6], subsequent observations revealed that other non vaccine injectables, i.e. drugs, foreign material, microchip implantation and trauma can also induce chronic inflammation, essential in the pathogenesis of FISS [2, 7,8,9]. However, chronic inflammation alone probably cannot induce neoplastic transformation [8, 10]. The exact pathogenesis of FISS is not fully understood and requires further research.

Metallothioneins (MTs; with the best characterised isoforms MT I and II) are a group of small cysteine-rich proteins, playing an important role in metal homeostasis and protection against heavy metal toxicity, DNA damage, oxidative stress, and apoptosis [11]. MT I-II also shows immunomodulatory effects by reducing the synthesis of pro-inflammatory cytokines and increasing the synthesis of anti-inflammatory cytokines [12]. These properties make MT I-II an interesting object of research, particularly in tumours arising in the background of chronic inflammation, irritation or injury. Due to its antioxidant and cytoprotective role, MT I-II expression can be responsible for tumour resistance to radiotherapy or chemotherapy [12,13,14,15]. As radiotherapy and – to a lesser extent – adjuvant chemotherapy, in addition to aggressive surgery, are used in treatment of FISS [16], the expression of MT I-II could be the potential predictive factor. Furthermore, as the chronic inflammation predispose to FISS, the possible downregulation of MT I-II (due to its antiinflammatory properties) could also play a role in the pathogenesis of FISS. In feline mammary gland tumours and cutaneous melanomas, increased expression of MT I-II was related to tumour progression [17]. The expression of metallothionein has not been previously investigated in FISS.

The aim of this study was to evaluate the expression of MT I-II in feline injection site fibrosarcomas and to investigate possible relationships between the expression of metallothionein, Ki67 index, inflammation score, necrosis score and tumour grade.

Results

Histological analysis of evaluated tumours is summarised in Table 1, and detailed characteristics of all evaluated tumours are presented in Supplementary Table 1. Five tumours were graded I (12.5%), 15 tumours—II (37.5%) and 20 tumours—III (50%). In tumours grade I, necrosis was either absent or involved less than 50% of the tumour parenchyma. Inflammatory infiltrates were absent or mild. In tumours grade II, necrosis was observed in only 40% of cases, and inflammatory infiltrates were variable. In tumours grade III, necrosis was observed in all cases, most of which involved more than 50% of the tumour parenchyma. Inflammatory infiltrates were massive in 75% of cases.

Table 1 Percentage of tumours grade I, II and III with particular mitotic, necrosis and inflammation scores, and IRS for MT expression (range, mean with standard deviation)

The mean Ki67 (Fig. 1A-C) index was 6.64 ± 3.31 in tumours grade I, 15.25 ± 5.36 in tumours grade II and 38.4 ± 14.4 in tumours grade III. Statistical analysis revealed that the Ki67 index was significantly higher in tumours grade III compared to grade II (p = 0.000) and to grade I (p = 0.000; Fig. 2A). Additionally, the Ki67 index was positively correlated with tumour grade (r = 0.853; p = 0.000; Fig. 2B), inflammation score (r = 0.452; p = 0.003; Fig. 2C), and necrosis score (r = 0.37; p = 0.018; Fig. 2D).

Fig. 1
figure 1

Feline injection site fibrosarcomas. A Tumour grade I. Small number of tumour cells show nuclear expression of Ki67. B Tumour grade II. Moderately numerous tumour cells show nuclear expression of Ki67. C Tumour grade III. Numerous tumour cells show nuclear expression of Ki67. Ki67 immunostaining with DAB, counterstaining with Mayer’s haematoxylin, 400x

Fig. 2
figure 2

Feline injection site fibrosarcomas. A Mean Ki67 index values in tumours grade I, II, and III. The Ki67 index was significantly higher in tumours grade III compared to grade II (p = 0.000) and I (p = 0.000). B Positive correlation between the Ki67 index and the tumour grade. The Ki67 index increased with the tumour grade (r = 0.853; p = 0.000). C Positive correlation between the Ki67 index and the inflammation score. The Ki67 index increased with the inflammation score (r = 0.452; p = 0.003). D Positive correlation between the Ki67 index and the necrosis score. The Ki67 index increases with the necrosis score (r = 0.37; p = 0.018)

The cytoplasmic and sometimes nuclear MT expression was observed in all tumours grade I (100%), 10 tumours grade II (66.67%), and 11 tumours grade III (55%) (Fig. 3A-C). The mean immunoreactive score (IRS) for MT expression was 6.2 ± 3.03, 1.87 ± 2.1, and 1.65 ± 2.18 for tumours grade I, II, and III, respectively. Statistical analysis showed that the IRS for MT expression was significantly higher in grade I compared to grade II (p = 0.04) and to grade III (p = 0.012; Fig. 4A). Moreover, IRS for MT expression was negatively correlated with tumour grade (r = -0.356; p = 0.024; Fig. 4B) and inflammation score (r = -0.713; p = 0.000; Fig. 4C). No correlation was found between IRS for MT expression and necrosis score (r = 0.014; p = 0.9; Fig. 4D).

Fig. 3
figure 3

Feline injection site fibrosarcomas. A Tumour grade I. Numerous tumour cells (quantitative score: 3) show moderate (qualitative score: 2) expression of metallothionein (IRS: 6). The expression is mostly cytoplasmic, but the nuclear expression is also present in some tumour cells. B Tumour grade II. Moderately numerous tumour cells (quantitative score: 2) show weak (qualitative score: 1) cytoplasmic expression of metallothionein (IRS: 2). C Tumour grade III. Absence of metallothionein expression in tumour cells. Metallothionein immunostaining with DAB, counterstaining with Mayer’s haematoxylin, 200x

Fig. 4
figure 4

Feline injection site fibrosarcomas. A Mean IRS for MT expression values in tumours grade I, II, and III. The IRS for MT expression was significantly higher in tumours grade I compared to grade II (p = 0.04) and III (p = 0.012). B Negative correlation between the IRS for MT expression and the tumour grade. The metallothionein expression decreased as the tumour grade was higher (r = -0.356; p = 0.024). C Negative correlation between the IRS for MT expression and the inflammation score. The metallothionein expression decreased as the inflammation score was higher (r = -0.713; p = 0.000). D No correlation was found between IRS for MT expression and necrosis score (r = 0.014; p = 0.9)

Discussion

We observed the expression of MT in 26 cases (out of 40) of feline injection site fibrosarcomas, and this expression was negatively correlated with the degree of inflammation and tumour grade. It was previously shown that MT has immunomodulatory properties, suppressing T-dependent humoral immune response [18] and function of cytotoxic T-cells [19]. The chronic inflammation is a key point in the pathogenesis of FISS. Free radicals generated during persistent inflammation cause DNA damage [20]. Furthermore, the degree of inflammatory infiltration is one of three parameters of a recently proposed grading system for feline soft tissue sarcomas [21]. Therefore, the negative correlation between MT expression and the degree of inflammatory infiltration (and tumour grade) in feline injection site fibrosarcomas indicates that the downregulation of MT expression may be involved in tumour progression. The downregulation of MT expression was observed in several human cancers, i.e. liver, colon and prostate [22,23,24]. In human colon carcinoma downregulation of a specific isoform of MT (MT1F) resulted from loss of heterozygosity [24]. As MT protects cells from oxidative stress, downregulation of MT expression might be linked to increased risk of DNA damage and mutagenic changes, responsible for carcinogenesis [17, 25] which is also very likely in feline injection site fibrosarcoma. On the contrary, a positive correlation between MT expression and tumour grade was found in selected human soft tissue sarcomas [26]. The elevated expression of MT allows tumour cells to evade the host immune response [19]. Furthermore, as the MT is responsible for resistance to radiotherapy [25], it can be assumed that feline injection site fibrosarcomas grade I could be possibly more resistant to radiotherapy (compared to grade II and III), but this relationship must be further evaluated in prospective clinical studies. Although MT expression was mainly cytoplasmic, we also observed nuclear expression in some tumour cells. The nuclear localization of MT is transiently observed during cell proliferation and early differentiation; this protein protects DNA from oxidative damage and apoptosis [27]. It was previously shown that nuclear expression of MT was responsible for cisplatin resistance in ovarian cancer [28].

The Ki67 index is associated with tumour proliferation, growth, and progression, and it is commonly used in human and veterinary medicine as a prognostic marker [29,30,31,32,33]. A high Ki67 index is associated with poor prognosis in several human and animal tumours, e.g., human and feline mammary gland tumours and human soft-tissue sarcomas [29, 34, 35]. In our study, the Ki67 index was positively correlated with tumour grade, but its prognostic significance must be elucidated in the further studies. Furthermore, we found a positive correlation between Ki67 index and inflammatory score. In a study on canine colorectal carcinoma, Ki67 index was positively correlated with the number of tumour associated macrophages and mast cells [36]. It is suggested that inflammatory cells have an impact on cancer development by increasing the invasive capacity, angiogenesis and motility of tumour cells [37]. In human breast cancer, the inflammation is closely associated with tumour proliferation and progression. This correlation may reflect an active immune response to poor tumour cell differentiation or may be a consequence of increased cytokine secretion by high-grade tumours [38]. The association between inflammatory infiltration and Ki67 index (as well as tumour grade) in feline injection site fibrosarcomas suggests that the inflammation plays an important role not only in pathogenesis, but also in tumour progression. Additionally, we found a positive correlation between Ki67 index and necrosis score. This is not surprising since tumour necrosis is a consequence of ischemic injury caused by rapid tumour growth [39]. Furthermore, necrotic cells release factors enhancing tumour cell proliferation [40]. In human breast cancer, the degree of the tumour necrosis reflects higher metabolic activity and more rapid growth, which results in higher Ki67 index in tumours with extent areas of necrosis [41].

Conclusion

The downregulation of MT expression in feline injection site fibrosarcomas is connected with an increase in the inflammatory infiltration. Both the reduction of MT expression and the increased degree of inflammatory infiltration seem to be associated with tumour progression.

Methods

Study design

The study included surgically excised cutaneous tumours collected from 40 cats between 2019–2020, 28 (70%) males and 12 (30%) females, aged 4–17 (mean: 11 ± 3 years). The samples were fixed in 10% neutral buffered formalin, processed routinely, embedded in paraffin wax, cut and stained with Mayer’s haematoxylin and eosin (HE). Inclusion criteria included morphological features [42, 43] and localisation in the injection site: interscapular region (50%; 20/40 cases), thigh (12.5%; 5/40 cases), flank (12.5%; 5/40 cases), lumbar area (10%; 4/40 cases), shoulder (10%; 4/40 cases), and dorsal area of the neck (5%; 2/40 cases). Histologically, the tumours were graded into grade I, II and III, according to the grading system proposed by Dobromylskyj et al. [21] for feline soft tissue sarcomas (Table 2). The number of inflammatory cells was categorised as none or mild (1), when inflammatory cells were absent or only few, scattered throughout the tumour parenchyma; moderate (2), when inflammatory cells were more numerous, forming distinct foci within the tumour parenchyma; and severe (3), when the inflammatory cells were numerous, and formed large foci. The necrosis extent was classified as 0 (no necrosis within the tumour), 1 (necrotic area up to 50% of tumour parenchyma) and 2 (necrotic area covers more than 50% of tumour parenchyma).

Table 2 Grading system for cutaneous soft tissue sarcomas [21]

Immunohistochemical evaluation

The sections for immunohistochemistry were mounted on silanized glass slides. Heat-induced antigen retrieval was performed in Tris–EDTA buffer pH 9.0 (EnVision™ Flex Target Retrieval Solution High pH, DAKO, Glostrup, Denmark) for 20 min at 96 °C using a PT-Link module (Dako, Glostrup, Denmark). Immunohistochemical examination of each tumour was performed using primary antibodies: Ki67 (monoclonal mouse anti-human, clone MIB-1, dilution 1:75, incubation time: 30 min in a humid chamber at room temperature; Dako, Glostrup, Denmark) and metallothionein (monoclonal mouse anti-metallothionein I-II, clone UC1MT, dilution 1:1000, incubation time: 60 min in a humid chamber at 60℃; Abcam, Cambridge, Great Britain) and a visualisation system based on the immunoperoxidase method, with 3,3-diaminobenzidine (DAB) as a substrate (EnVision + System-HRP, Mouse, Dako, Glostrup, Denmark). The slides were counterstained with Mayer’s haematoxylin. Positive and negative control slides were processed together with the evaluated slides (metallothionein – feline mammary gland, Ki67 – feline skin). Brown precipitate at the antigen site was regarded as a positive reaction (Ki67 – nuclear; MT I-II – nuclear and cytoplasmic). The slides were evaluated under a light microscope (BX63, Olympus, Tokyo, Japan) using CellSense (Olympus, Tokyo, Japan) software.

Ki67 evaluation

The expression of Ki67 was calculated in 10 HPFs (high power fields, 400x), in areas with the most numerous positive cells (“hot-spots”), avoiding areas of inflammation and necrosis The Ki67 index was expressed as a percentage of positive cells and was obtained by calculating the ratio of positively stained tumour cells and all tumour cells observed in the analysed microscopic fields, as was previously described by Patruno et al. [32]. Mean values (with standard deviation) were calculated for groups with grades I, II and III.

MT evaluation

The expression of MT was assessed in 10 randomly selected HPFs (400x), using a semiquantitative scale that included the intensity of the immunostaining (0: none; 1: weak; 2: moderate; 3: intense) and the percentage of immunoreactive tumour cells (1: < 10%; 2: 10–50%; 3: 51–80%; 4: > 80%). IRS for MT expression was a product of multiplication of points given for individual traits and ranged between 0 and 12 [44,45,46,47]. Mean values (with standard deviation) were calculated for groups with grades I, II and III.

Statistical analysis

The variables were checked for normality using the Shapiro–Wilk test. Differences in Ki67 index and IRS for MT expression between groups with grade I, II and III were analysed using Kruskal‒Wallis H test (one-way ANOVA on ranks) followed by Dunn’s post-hoc test. Correlations between tumour grade, inflammation score, necrosis score, Ki67 index and IRS for MT expression were examined using Spearman’s rank correlation (r: Spearman’s rank correlation coefficient); p < 0.05 was considered statistically significant, and p < 0.001 as highly significant. The statistical analysis was performed using Statistica 14 software (StatSoft Inc., Tulsa, OK, USA).

Availability of data and materials

Data used in this study are available from the corresponding author on reasonable request.

References

  1. Martano M, Morello E, Buracco P. Feline injection-site sarcoma: past, present and future perspectives. Vet J. 2011;188:136–41.

    Article  PubMed  Google Scholar 

  2. Porcellato I, Menchetti L, Brachelente C, Sforna M, Raginato A, Lepri E, Mechelli L. Feline Injection-Site Sarcoma: Matrix Remodeling and Prognosis. Vet Pathol. 2017;54:204–11.

    Article  CAS  PubMed  Google Scholar 

  3. Hartmann K, Day MJ, Thiry E, Lloret A, Frymus T, Addie D, Boucraut-Baralon C, Egberink H, Gruffydd-Jones T, Horzinek MC, Hosie MJ, Lutz H, Marsilio F, Pennisi MG, Radford AD, Truyen U, Möstl K, European Advisory Board on Cat Diseases. Feline injection-site sarcoma: ABCD guidelines on prevention and management. J Feline Med Surg. 2015;17:606–13.

    Article  PubMed  Google Scholar 

  4. Hendrick MJ, Dunagan CA. Focal necrotizing granulomatous panniculitis associated with subcutaneous injection of rabies vaccine in cats and dogs: 10 cases (1988–1989). J Am Vet Med Assoc. 1991;198:304–5.

    CAS  PubMed  Google Scholar 

  5. Hendrick MJ, Goldschmidt MH. Do injection site reactions induce fibrosarcomas in cats? J Am Vet Med Assoc. 1991;199:968.

    CAS  PubMed  Google Scholar 

  6. Kass PH, Barnes WG Jr, Spangler WL, Chomel BB, Culbertson MR. Epidemiologic evidence for a causal relation between vaccination and fibrosarcoma tumorigenesis in cats. J Am Vet Med Assoc. 1993;203:396–405.

    CAS  PubMed  Google Scholar 

  7. Esplin DG, Bigelow M, McGill LD, Wilson SR. Fibrosarcoma at the site of a lufenuron injection in a cat. Vet Cancer Soc Newsletter. 1999;23:8–9.

    Google Scholar 

  8. Kass PH, Spangler WL, Hendrick MJ, McGill LD, Esplin DG, Lester S, Slater M, Meyer EK, Boucher F, Peters EM, Gobar GG, Htoo T, Decile K. Multicenter case-control study of risk factors associated with development of vaccine-associated sarcomas in cats. J Am Vet Med Assoc. 2003;223:1283–92.

    Article  PubMed  Google Scholar 

  9. Munday JS, Banyay K, Aberdein D, French AF. Development of an injection site sarcoma shortly after meloxicam injection in an unvaccinated cat. J Feline Med Surg. 2011;13:988–91.

    Article  PubMed  Google Scholar 

  10. Carminato A, Vascellari M, Marchioro W, Melchiotti E, Mutinelli F. Microchip-associated fibrosarcoma in a cat. Vet Dermatol. 2011;22:565–9.

    Article  PubMed  Google Scholar 

  11. Si M, Lang J. The roles of metallothioneins in carcinogenesis. J Hematol Oncol. 2018;11:107.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Pedersen MØ, Larsen A, Stoltenberg M, Penkowa M. The role of metallothionein in oncogenesis and cancer prognosis. Prog Histochem Cytochem. 2009;44:29–64.

    Article  CAS  PubMed  Google Scholar 

  13. Lynn NN, Howe MC, Hale RJ, Collins GN, O’Reilly PH. Over expression of metallothionein predicts resistance of transitional cell carcinoma of bladder to intravesical mitomycin therapy. J Urol. 2003;169:721–3.

    Article  CAS  PubMed  Google Scholar 

  14. Smith DJ, Jaggi M, Zhang W, Galich A, Du C, Sterrett SP, Smith LM, Balaji KC. Metallothioneins and resistance to cisplatin and radiation in prostate cancer. Urology. 2006;67:1341–7.

    Article  PubMed  Google Scholar 

  15. Mairinger FD, Schmeller J, Borchert S, Wessolly M, Mairinger E, Kollmeier J, Hager T, Mairinger T, Christoph DC, Walter RFH, Eberhardt WEE, Plönes T, Wohlschlaeger J, Jasani B, Schmid KW, Bankfalvi A. Immunohistochemically detectable metallothionein expression in malignant pleural mesotheliomas is strongly associated with early failure to platin-based chemotherapy. Oncotarget. 2018;9:22254–68.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Zabielska-Koczywąs K, Wojtalewicz A, Lechowski R. Current knowledge on feline injection-site sarcoma treatment. Acta Vet Scand. 2017;59:47.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Dincer Z, Jasani B, Haywood S, Mullins JE, Fuentealba IC. Metallothionein expression in canine and feline mammary and melanotic tumours. J Comp Pathol. 2001;125:130–6.

    Article  CAS  PubMed  Google Scholar 

  18. Canpolat E, Lynes MA. In Vivo Manipulation of Endogenous Metallothionein with a Monoclonal Antibody Enhances a T-Dependent Humoral Immune Response. Toxicol Sci. 2001;62:61–70.

    Article  CAS  PubMed  Google Scholar 

  19. Youn J, Lynes MA. Metallothionein-induced suppression of cytotoxic T lymphocyte function: an important immunoregulatory control. Toxicol Sci. 1999;52:199–208.

    Article  CAS  PubMed  Google Scholar 

  20. Woodward KN. Origins of injection-site sarcomas in cats: the possible role of chronic inflammation-a review. ISRN Vet Sci. 2011;12:210982.

    Google Scholar 

  21. Dobromylskyj MJ, Richards V, Smith KC. Prognostic factors and proposed grading system for cutaneous and subcutaneous soft tissue sarcomas in cats, based on a retrospective study. J Feline Med Surg. 2021;23:168–74.

    Article  PubMed  Google Scholar 

  22. Datta J, Majumder S, Kutay H, Motiwala T, Frankel W, Costa R, Cha HC, MacDougald OA, Jacob ST, Ghoshal K. Metallothionein expression is suppressed in primary human hepatocellular carcinomas and is mediated through inactivation of CCAAT/enhancer binding protein alpha by phosphatidylinositol 3-kinase signaling cascade. Cancer Res. 2007;67:2736–46.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Wei H, Desouki MM, Lin S, Xiao D, Franklin RB, Feng P. Differential expression of metallothioneins (MTs) 1, 2, and 3 in response to zinc treatment in human prostate normal and malignant cells and tissues. Mol Cancer. 2008;7:7.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Yan DW, Fan JW, Yu ZH, Li MX, Wen YG, Li DW, Zhou CZ, Wang XL, Wang Q, Tang HM, Peng ZH. Downregulation of metallothionein 1F, a putative oncosuppressor, by loss of heterozygosity in colon cancer tissue. Biochim Biophys Acta. 2012;1822:918–26.

    Article  CAS  PubMed  Google Scholar 

  25. Takahashi S. Positive and negative regulators of the metallothionein gene (Review). Mol Med Rep. 2015;12:795–9.

    Article  CAS  PubMed  Google Scholar 

  26. Dziegiel P, Salwa-Zurawska W, Zurawski J, Wojnar A, Zabel M. Prognostic significance of augmented metallothionein (MT) expression correlated with Ki-67 antigen expression in selected soft tissue sarcomas. Histol Histopathol. 2005;20:83–9.

    CAS  PubMed  Google Scholar 

  27. Cherian MG, Apostolova MD. Nuclear localization of metallothionein during cell proliferation and differentiation. Cell Mol Biol (Noisy-le-grand). 2000;46:347–56.

    CAS  PubMed  Google Scholar 

  28. Surowiak P, Materna V, Maciejczyk A, Pudełko M, Markwitz E, Spaczyński M, Dietel M, Zabel M, Lage H. Nuclear metallothionein expression correlates with cisplatin resistance of ovarian cancer cells and poor clinical outcome. Virchows Arch. 2007;450:279–85.

    Article  CAS  PubMed  Google Scholar 

  29. Inwald EC, Klinkhammer-Schalke M, Hofstädter F, Zeman F, Koller M, Gerstenhauer M, Ortmann O. Ki-67 is a prognostic parameter in breast cancer patients: results of a large population-based cohort of a cancer registry. Breast Cancer Res Treat. 2013;139:539–52.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Klöppel G, La Rosa S. Ki67 labeling index: assessment and prognostic role in gastroenteropancreatic neuroendocrine neoplasms. Virchows Arch. 2018;472:341–9.

    Article  PubMed  Google Scholar 

  31. Sierra Matiz OR, Santilli J, Anai LA, Da Silva MCL, Sueiro FA, Sequeira JL, Magalhães LF, Magalhães GM, Tinucci Costa M, Calazans SG. Prognostic significance of Ki67 and its correlation with mitotic index in dogs with diffuse large B-cell lymphoma treated with 19-week CHOP-based protocol. J Vet Diagn Invest. 2018;30:263–7.

    Article  CAS  PubMed  Google Scholar 

  32. Patruno R, Passantino G, Laface C, Tinelli A, Zito A, Ruggieri R, Luposella F, Gadaleta P, Laforgia M, Lacitignola L, Ammendola M, Ranieri G, Zizzo N. Microvascular Density, Endothelial Area, and Ki-67 Proliferative Index Correlate Each Other in Cat Post-Injection Fibrosarcoma. Cells. 2020;10:31.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Travaglino A, Raffone A, Catena U, De Luca M, Toscano P, Del Prete E, Vecchione ML, Lionetti R, Zullo F, Insabato L. Ki67 as a prognostic marker in uterine leiomyosarcoma: a quantitative systematic review. Eur J Obstet Gynecol Reprod Biol. 2021;266:119–24.

    Article  CAS  PubMed  Google Scholar 

  34. Sorbye SW, Kilvaer TK, Valkov A, Donnem T, Smeland E, Al-Shibli K, Bremnes RM, Busund LT. Prognostic impact of Jab1, p16, p21, p62, Ki67 and Skp2 in soft tissue sarcomas. PLoS One. 2012;10:e47068.

    Article  Google Scholar 

  35. Soares M, Ribeiro R, Carvalho S, Peleteiro M, Correia J, Ferreira F. Ki-67 as a Prognostic Factor in Feline Mammary Carcinoma: What Is the Optimal Cutoff Value? Vet Pathol. 2016;53:37–43.

    Article  CAS  PubMed  Google Scholar 

  36. Woldemeskel M, Hawkins I, Whittington L. Ki-67 protein expression and tumor associated inflammatory cells (macrophages and mast cells) in canine colorectal carcinoma. BMC Vet Res. 2017;20:111.

    Article  Google Scholar 

  37. Coussens LM, Werb Z. Inflammation and cancer. Nature. 2002;6917:860–7.

    Article  Google Scholar 

  38. Murri A, Hilmy M, Bell J, Willson C, McNicol A-M, Lannigan A, Doughty JC, McMillan DC. The relationship between the systemic inflammatory response, tumour proliferative activity, T-lymphocytic and macrophage infiltration, microvessel density and survival in patients with primary operable breast cancer. Br J Cancer. 2008;99:1013–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Caruso RA, Branca G, Fedele F, Irato E, Finocchiaro G, Parisi A, Ieni A. Mechanisms of coagulative necrosis in malignant epithelial tumors (Review). Oncol Lett. 2014;8:1397–402.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Yee PP, Li W. Tumor necrosis: a synergistic consequence of metabolic stress and inflammation. BioEssays. 2021;43:e2100029.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Bahaddin MM. A comparative study between Ki67 positive versus Ki67 negative females with breast cancer: cross sectional study. Ann Med Surg (Lond). 2020;60:232–5.

    Article  PubMed  Google Scholar 

  42. Doddy FD, Glickman LT, Glickman NW, Janovitz EB. Feline fibrosarcomas at vaccination sites and non-vaccination sites. J Comp Pathol. 1996;114:165–74.

    Article  CAS  PubMed  Google Scholar 

  43. Dean RS, Pfeiffer DU, Adams VJ. The incidence of feline injection site sarcomas in the United Kingdom. BMC Vet Res. 2013;9:17.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Remmele W, Stegner HE. Recommendation for uniform definition of an immunoreactive score (IRS) for immunohistochemical estrogen receptor detection (ER-ICA) in breast cancer tissue. Pathologe. 1987;8:138–40.

    CAS  PubMed  Google Scholar 

  45. Surowiak P, Matkowski R, Materna V, Györffy B, Wojnar A, Pudelko M, Dziegiel P, Kornafel J, Zabel M. Elevated metallothionein (MT) expression in invasive ductal breast cancers predicts tamoxifen resistance. Histol Histopathol. 2005;20:1037–44.

    CAS  PubMed  Google Scholar 

  46. Nowak M, Madej JA, Dziegiel P. Extent of metallothionein expression in correlation with expression of KI-67 antigen in soft tissue fibrosarcomas in dogs. Bull Vet Inst Pulawy. 2007;51:139–44.

    Google Scholar 

  47. Mikiewicz M, Otrocka-Domagała I, Paździor-Czapula K, Gesek M. Morphology and immunoreactivity of canine and feline extramedullary plasmacytomas. Pol J Vet Sci. 2016;19:345–52.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We would like to thank Cezary Zwoliński and Dominika Piech for preparing the archival specimens.

Funding

Project financially supported by the Minister of Education and Science under the program entitled "Regional Initiative of Excellence" for the years 2019–2023, Project No. 010/RID/2018/19, amount of funding 12.000.000 PLN; the National Science Center, project No. 2021/05/X/NZ4/00037.

Author information

Authors and Affiliations

Authors

Contributions

Mateusz Mikiewicz designed and performed the experiments, analysed the data, and wrote the manuscript; Katarzyna Paździor-Czapula edited the manuscript; Joanna Fidorowicz collected samples; Michał Gesek contributed to data analysis and graphs preparation; Iwona Otrocka-Domagała supervised and corrected the manuscript. The authors read and approved the final manuscript.

Corresponding author

Correspondence to Mateusz Mikiewicz.

Ethics declarations

Ethics approval and consent to participate

Ethics approval is not applicable under the Act of 15 January 2015 on the protection of animals used for scientific or educational purposes – Journal of Laws of the Republic of Poland (Journal of Laws 2015 item 266) and Local Ethics Committee for Animal Experiments. The study used archival specimens collected in the Department of Pathological Anatomy. Written informed consent was obtained from the owner or legal custodian of all animals described in this work for the procedures undertaken in this retrospective study. No animals or humans are identifiable within this publication, and therefore additional informed consent for publication was not required.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1:

Supplementary Table 1. Detailed characteristics of evaluated feline injection site fibrosarcomas.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Mikiewicz, M., Paździor-Czapula, K., Fiedorowicz, J. et al. Metallothionein expression in feline injection site fibrosarcomas. BMC Vet Res 19, 42 (2023). https://doi.org/10.1186/s12917-023-03604-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12917-023-03604-5

Keywords