The current study was directed to investigation on the molecules, as well as different intra- and extra-cellular interactions between them, underlining the regulatory mechanisms, preventing the development of malignancies, neuro-degenerative and neuro-psychiatric disorders, by appropriate in vivo- and in vitro-experimental models. Significantly higher frequency of the spontaneous chromosomal fragility in the patients was established compared to the controls, including in the centromere regions of the chromosomes. The increased centromere spontaneous chromosomal fragility predisposes to abnormal cellular division due to injured interaction with the mitotic spindle, and thus – to number chromosomal aberrations. On the other hand, this increased frequency of the spontaneous chromosomal fragility suggests abnormal structure of the respective chromosomal/chromatin components and thus, an increased risk about gene mutations and structural chromosomal aberrations. Additionally, the microtubule-associated proteins (MAPs) abnormal structure is a reason about the predisposition to these pathologies. These inter-molecular interactions were proposed as underlining the functions of the different cells, tissues, organs, as well as in various time periods and in different organisms. Furthermore, a possibility about production of antibodies/immunoglobulins by non-lymphoid types of cells, tissues and organs in appropriate circumstances was shown. Because the so produced antibodies are out of the germinative centers in the specialized lymphoid tissues and organs, the control of their functions by small molecules as gangliosides is very important. The activity of the tumor-suppressor genes and their protein products should be directed to protection besides against malignancies, also against other diseases and disorders as degenerative pathologies.