A. MDA-MB-231 were incubated with CD44 and CD49f siRNAs, and their respective transcript expression levels were monitored. The ability of MDA-MB-231 cells to form mammospheres was challenged by knocking down CD44, CD49f, and YB-1 individually with their corresponding siRNAs prior to seeding into the assay. B. Stable G418-selected lines of MDA-MB-231 and SUM 149 cells expressing Flag:EV, Flag:YB-1WT, Flag:YB-1S102D were also assayed for their abilities to form mammospheres. The Flag:YB-1S102D lines of both cell lines were first subjected to CD44 and CD49f siRNA treatments and their mammosphere-forming abilities quantified. Further, SUM 149 Flag:EV, Flag:YB-1WT, Flag:YB-1S102D cells were serially passaged in mammosphere cultures. After 7 days in culture, the spheres were counted, dissociated into single cells, and re-seeded into the mammosphere assay. The yield of dissociated single cells obtained after 7 days in secondary non-adherent cultures were analyzed as a measure of self-renewal. C. The functional roles of both receptors in anchorage-independent growth were analyzed in a soft agar assay by single CD44 or CD49f gene knockdowns. MDA-MB-231 Flag:EV, Flag:YB-1WT, Flag:YB-1S102D cells, as well as Flag:YB-1S102D cells treated with Control, CD44 or CD49f siRNAs, were also examined for their ability to form colonies in soft agar subsequent to the gene knockdowns. D. MDA-MB-231 cell growth in Matrigel was challenged by pre-treating the cells with YB-1, CD44, and CD49f siRNA oligonucleotides. Photographs were taken on Day 7 after cell seeding into Matrigel.