Bone tumours are biologically diverse and complex, although bone metastases or secondary bone cancers are very common after lung and liver cancer. Fortunately, primary bone cancers, which originates in the bone, are rare [1] thus, less studies focued on primary bone cancers compared to other cancers [2]. Primary bone cancers are classified into 15 different categories including cartilage, osteogenic, fibrogenic, fibrohistiocytic, hematopoietic, giant cell, notochordal, smooth muscle, vascular, lipogenic and neurological, Ewing sarcoma / primary neuroectodermal tumour, miscellaneous tumours, and joint lesions [3, 4, 5]. Osteosarcoma (35%), chondrosarcoma (30%), and Ewing sarcoma (16%) are the most common forms of bone cancers. Malignant fibrocystic histiocytoma, fibrosarcoma, chordoma, and giant cell tumours accounts as a less prevalent tumours which compromise 1–5% of all primary malignant bone tumours [6]. Hydatid cyst, which is the larval stage of the cestode worm Echinococcus granulosus, is a common parasitic infection affecting human and animals. E.granulous cyst composed of different layers in which the last external layer, laminated layer (LL), has a carbohydrate-rich structure that protects the parasite against the destruction by host immune system molecules [7]. Cancer cells and parasites shared some common features and the presence of similar antigens between them has been reported; in he other hand, it has been postulated that some parasites may have anti-cancer activities due to having similar antigene there fore, administrating the paprasite anitgens as target for cancer immunotherapy have been gain the attraction [8] Some parasites such as Trypanosoma cruzi (T. cruzi), Toxoplasma gondii (T. gondii), Toxocara Canis, Acanthamoeba castellani, and plasmodium Yoelii have been showed to have a anticancer activity in the experimental animals [9, 10, 11] henece some parasites such as T. cruzi, Echinococcus granulosus (E. granulosus) and T. gondii shared a similar carcinogen antigenes such as the presence of the cancer-associated mucin-type O-glycans in hydatid cyst [12, 13]. So it is suggested that E. granulosus larva may induce anticancer effect through activating the host immune response [14], for example, a mucin-type-O-glycans (glycosylated 27 kDa molecule) pf this helminth is similar to human breast cancer antigens and can introduce to the host immune system for later protection against cancer [15]. In liver and lung hydatidosis, induce seceration of cytokines (IFN, TNF-α, and IL-6) [16] contributing host immune defence against tumours. Also, several Echinococcus antigens can induce antibody-mediated immunity, that can establish non-specific immunity against some cancer [17]. Inquiries show an immunological association between the laminated layer of hydatid cyst and different cancer cells, therefore in this study, antigens similarity between hydatid cyst and different bone cancers were evaluated.