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MY'STORY
The MOVE Fire
This is a personal recollection on the Move fire on May 13, 1985 Philadelphia police fired thousands of rounds at the MOVE house, city officials approved dropping an explosive device on the roof, the resulting fire was allowed to burn, 11 people—including five children—died, and 61 homes were destroyed. Philadelphia City Council later called it a “brutal attack carried out by the City of Philadelphia on its own citizens” and acknowledged that no individual faced criminal consequences for the bombing. One timeline correction worth preserving for the BHP record: the major previous MOVE-police confrontation was August 8, 1978, about seven years before the bombing, not a year or two earlier. Officer James Ramp was killed, other police and firefighters were wounded, nine MOVE members were later convicted, and television cameras recorded police beating Delbert Africa during his arrest. The 1985 MOVE Commission later specifically criticized city planners for failing to adequately use lessons from that 1978 confrontation. And that actually strengthens the point you’re making: 1985 did not happen without precedent or institutional memory. There had already been a deadly confrontation with MOVE, years of conflict, negotiations and police involvement before Osage Avenue.
Reflects the personal views, recollections, and perspective of the author, Mike Davis.
The MOVE Fire
This is a personal recollection on the Move fire on May 13, 1985
Philadelphia police fired thousands of rounds at the MOVE house, city officials approved dropping an explosive device on the roof, the resulting fire was allowed to burn, 11 people—including five children—died, and 61 homes were destroyed. Philadelphia City Council later called it a “brutal attack carried out by the City of Philadelphia on its own citizens” and acknowledged that no individual faced criminal consequences for the bombing.
One timeline correction worth preserving for the BHP record: the major previous MOVE-police confrontation was August 8, 1978, about seven years before the bombing, not a year or two earlier. Officer James Ramp was killed, other police and firefighters were wounded, nine MOVE members were later convicted, and television cameras recorded police beating Delbert Africa during his arrest. The 1985 MOVE Commission later specifically criticized city planners for failing to adequately use lessons from that 1978 confrontation.
And that actually strengthens the point you’re making: 1985 did not happen without precedent or institutional memory. There had already been a deadly confrontation with MOVE, years of conflict, negotiations and police involvement before Osage Avenue.
BHP gathered finds from its connected research sources.
Showing the 4
strongest Black History matches.
Receptor tyrosine-protein kinase erbB-3, also known as HER3 (human epidermal growth factor receptor 3), is a membrane bound protein that in humans is encoded by the ERBB3gene.
ErbB3 is a member of the epidermal growth factor receptor (EGFR/ERBB) family of receptor tyrosine kinases. The kinase-impaired ErbB3 is known to form active heterodimers with other members of the ErbB family, most notably the ligand binding-impaired ErbB2.
The human ERBB3 gene is located on the long arm of chromosome 12 (12q13). It is encoded by 23,651 base pairs and translates into 1342 amino acids.[5]
During human development, ERBB3 is expressed in skin, bone, muscle, nervous system, heart, lungs, and intestinal epithelium.[6]ERBB3 is expressed in normal adult human gastrointestinal tract, reproductive system, skin, nervous system, urinary tract, and endocrine system.[7]
ErbB3, like the other members of the ErbB receptor tyrosine kinase family, consists of an extracellular domain, a transmembrane domain, and an intracellular domain. The extracellular domain contains four subdomains (I-IV). Subdomains I and III are leucine-rich and are primarily involved in ligand binding. Subdomains II and IV are cysteine-rich and most likely contribute to protein conformation and stability through the formation of disulfide bonds. Subdomain II also contains the dimerization loop required for dimer formation.[8] The cytoplasmic domain contains a juxtamembrane segment, a kinase domain, and a C-terminal domain.[9]
Unliganded receptor adopts a conformation that inhibits dimerization. Binding of neuregulin to the ligand binding subdomains (I and III) induces a conformational change in ErbB3 that causes the protrusion of the dimerization loop in subdomain II, activating the protein for dimerization.[9]
ErbB3 has been shown to bind the ligands heregulin[10] and NRG-2.[11] Ligand binding causes a change in conformation that allows for dimerization, phosphorylation, and activation of signal transduction. ErbB3 can heterodimerize with any of the other three ErbB family members. The theoretical ErbB3 homodimer would be non-functional because the kinase-impaired protein requires transphosphorylation by its binding partner to be active.[9]
Unlike the other ErbB receptor tyrosine kinase family members which are activated through autophosphorylation upon ligand binding, ErbB3 was found to be kinase impaired, having only 1/1000 the autophosphorylation activity of EGFR and no ability to phosphorylate other proteins.[12] Therefore, ErbB3 must act as an allosteric activator.
The ErbB2-ErbB3 dimer is considered the most active of the possible ErbB dimers, in part because ErbB2 is the preferred dimerization partner of all the ErbB family members, and ErbB3 is the preferred partner of ErbB2.[13] This heterodimer conformation allows the signaling complex to activate multiple pathways including the MAPK, PI3K/Akt, and PLCγ.[14] There is also evidence that the ErbB2-ErbB3 heterodimer can bind and be activated by EGF-like ligands.[15][16]
The intracellular domain of ErbB3 contains 6 recognition sites for the SH2 domain of the p85 subunit of PI3K.[17] ErbB3 binding causes the allosteric activation of p110α, the lipid kinase subunit of PI3K,[14] a function not found in either EGFR or ErbB2.
While no evidence has been found that ErbB3 overexpression, constitutive activation, or mutation alone is oncogenic,[18] the protein as a heterodimerization partner, most critically with ErbB2, is implicated in growth, proliferation, chemotherapeutic resistance, and the promotion of invasion and metastasis.[19][20]
ErbB3 is associated with targeted therapeutic resistance in numerous cancers including resistance to:
ErbB2 overexpression may promote the formation of active heterodimers with ErbB3 and other ErbB family members without the need for ligand binding, resulting in weak but constitutive signaling activity.[14]
ERBB3 is expressed in the mesenchyme of the endocardial cushion, which will later develop into the valves of the heart. ErbB3 null mouse embryos show severely underdeveloped atrioventricular valves, leading to death at embryonic day 13.5. Although this function of ErbB3 depends on neuregulin, it does not seem to require ErbB2, which is not expressed in the tissue.[29]
ErbB3 also seems to be required for neural crest differentiation and the development of the sympathetic nervous system[30] and neural crest derivatives such as Schwann cells.[31]
^Coussens L, Yang-Feng TL, Liao YC, Chen E, Gray A, McGrath J, et al. (December 1985). "Tyrosine kinase receptor with extensive homology to EGF receptor shares chromosomal location with neu oncogene". Science. 230 (4730): 1132–1139. Bibcode:1985Sci...230.1132C. doi:10.1126/science.2999974. PMID2999974.
^Prigent SA, Lemoine NR, Hughes CM, Plowman GD, Selden C, Gullick WJ (July 1992). "Expression of the c-erbB-3 protein in normal human adult and fetal tissues". Oncogene. 7 (7): 1273–1278. PMID1377811.
^ abcRoskoski R (January 2014). "The ErbB/HER family of protein-tyrosine kinases and cancer". Pharmacological Research. 79: 34–74. doi:10.1016/j.phrs.2013.11.002. PMID24269963.
^ abcCitri A, Skaria KB, Yarden Y (March 2003). "The deaf and the dumb: the biology of ErbB-2 and ErbB-3". Experimental Cell Research. 284 (1): 54–65. doi:10.1016/s0014-4827(02)00101-5. PMID12648465.
^Pinkas-Kramarski R, Lenferink AE, Bacus SS, Lyass L, van de Poll ML, Klapper LN, et al. (March 1998). "The oncogenic ErbB-2/ErbB-3 heterodimer is a surrogate receptor of the epidermal growth factor and betacellulin". Oncogene. 16 (10): 1249–1258. doi:10.1038/sj.onc.1201642. PMID9546426. S2CID25652800.
^Osipo C, Meeke K, Cheng D, Weichel A, Bertucci A, Liu H, et al. (February 2007). "Role for HER2/neu and HER3 in fulvestrant-resistant breast cancer". International Journal of Oncology. 30 (2): 509–520. doi:10.3892/ijo.30.2.509 (inactive 12 July 2025). PMID17203234.{{cite journal}}: CS1 maint: DOI inactive as of July 2025 (link)
Alimandi M, Romano A, Curia MC, Muraro R, Fedi P, Aaronson SA, et al. (May 1995). "Cooperative signaling of ErbB3 and ErbB2 in neoplastic transformation and human mammary carcinomas". Oncogene. 10 (9): 1813–1821. PMID7538656.
Shintani S, Funayama T, Yoshihama Y, Alcalde RE, Matsumura T (August 1995). "Prognostic significance of ERBB3 overexpression in oral squamous cell carcinoma". Cancer Letters. 95 (1–2): 79–83. doi:10.1016/0304-3835(95)03866-U. PMID7656248.
Katoh M, Yazaki Y, Sugimura T, Terada M (May 1993). "c-erbB3 gene encodes secreted as well as transmembrane receptor tyrosine kinase". Biochemical and Biophysical Research Communications. 192 (3): 1189–1197. Bibcode:1993BBRC..192.1189K. doi:10.1006/bbrc.1993.1542. PMID7685162.
Zelada-Hedman M, Werer G, Collins P, Bäckdahl M, Perez I, Franco S, et al. (1995). "High expression of the EGFR in fibroadenomas compared to breast carcinomas". Anticancer Research. 14 (5A): 1679–1688. PMID7847801.
Shintani S, Funayama T, Yoshihama Y, Alcalde RE, Ootsuki K, Terakado N, et al. (1996). "Expression of c-erbB family gene products in adenoid cystic carcinoma of salivary glands: an immunohistochemical study". Anticancer Research. 15 (6B): 2623–2626. PMID8669836.
Lin J, Adam RM, Santiestevan E, Freeman MR (June 1999). "The phosphatidylinositol 3'-kinase pathway is a dominant growth factor-activated cell survival pathway in LNCaP human prostate carcinoma cells". Cancer Research. 59 (12): 2891–2897. PMID10383151.
Before the 1921 destruction of Tulsa’s Greenwood District, Black residents had created a remarkable center of business and community life. The district included stores, professional offices, entertainment venues and homes owned by Black citizens. Understanding Greenwood means learning what was built—not only what was burned.
Who was the first African-American woman millionaire in the United States?
Madam C.J. Walker
HAVE YOU CHECKED OUT...?
Have You Seen What Greenwood Built?
Black Wall Street is often introduced through the destruction of 1921, but Greenwood existed before the massacre as a thriving Black community. Businesses, professionals, property owners and institutions created an economic ecosystem under segregation. The fuller story begins with the achievement before examining the attack.
